Ndc 57844 130 01 - segments of the NDC number, separated by hyphens per FDA website. o In the Open Payments application, this element corresponds to the “ National Drug Code (NDC) of Associated Covered Drug or Biological” field for PY2013 – PY2015 submissions or the “Associated Drug or Biological NDC” field for PY2016 onward submissions. • ProprietaryName

 
National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... . Lab 9 5 create mobile device connections

National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... The initial dosage of Dexamethasone Sodium Phosphate Injection, USP may vary from 0.5 mg/day to 9 mg/day depending on the specific disease entity ... HOW SUPPLIED. Dexamethasone Sodium Phosphate Injection, USP is a sterile, clear, colorless solution, essentially free from visible particles and is supplied as follows: 10 mg per mL - 1 mL Single ...Adderall immediate release tablet, Teva, 5 mg, bottle, 100 count, NDC 57844-0105-01 Adderall immediate release tablet, Teva, 7.5 mg, bottle, 100 count, NDC 57844-0117-01 Amphetamine mixed salts immediate release tablet, Alvogen, 10 mg, bottle, 100 count, NDC 47781-0176-01National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... May 30, 2023 · NDC 57844-105-01. Adderall ® CII ... NDC:57844-130-01: 100 TABLET in 1 BOTTLE: None: Marketing Information: Marketing Category: Application Number or Monograph Citation: The initial dosage of Dexamethasone Sodium Phosphate Injection, USP may vary from 0.5 mg/day to 9 mg/day depending on the specific disease entity ... HOW SUPPLIED. Dexamethasone Sodium Phosphate Injection, USP is a sterile, clear, colorless solution, essentially free from visible particles and is supplied as follows: 10 mg per mL - 1 mL Single ...Apr 20, 2022 · Pharmacokinetics. Mixed Salts of a Single Entity Amphetamine Product contain d-amphetamine and l-amphetamine salts in the ratio of 3:1. Following administration of a single dose 10 or 30 mg of Mixed Salts of a Single Entity Amphetamine Product to healthy volunteers under fasted conditions, peak plasma concentrations occurred approximately 3 hours post-dose for both d-amphetamine and l-amphetamine. SEARCH RESULTS for: 1009145 [RxCUI] (22 results) Share package ndc active ingredients active ingredients info ... .01 mg/1 ml; 1.2 mg/1 ml 250 ml in 1 cartridge ... 130 vial in 1 vial, piggyback > 130 injection, powder, for solution in 1 vial ...Manufacturer/ NDC Number CPT Code: CVX Code Combination Vaccines Pediarix (VFC) DTAP-Hep B-IPV Birth - 6 years : 0.5 ml IM: GlaxoSmithKline – SKB NDC: 58160-0811-52 90723: 110 Pentacel (VFC) DTaP-Hib-IPV Birth - 4 years: 0.5 ml IM: Sanofi Pasteur – PMC NDC: 49281-0510-05 90698: 120 Kinrix (VFC) DTaP-IPV 4 - 6 years: 0.5 ml IM ...Mar 10, 2022 · 3/10/2022 Amphetamine Mixed Salts, Immediate-Release Tablets Products Affected - Description Amphetamine mixed salts immediate release tablet, Mylan, 12.5 mg, bottle, 100 count, NDC 00378-4544-01 - discontinued Amphetamine mixed salts immediate release tablet, Mylan, 15 mg, bottle, 100 count, NDC 00378-4545-01 - discontinued Mar 10, 2022 · Adderall immediate release tablet, Teva, 5 mg, bottle, 100 count, NDC 57844-0105-01 Adderall immediate release tablet, Teva, 7.5 mg, bottle, 100 count, NDC 57844-0117-01 Amphetamine mixed salts immediate release tablet, Mallinckrodt, 10 mg, bottle, 100 count, NDC 00406-8892-01 They are available in bottles of 100 tablets (NDC 57844-130-01). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).SEARCH RESULTS for: 577957 [RxCUI] (24 results) ShareNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Product Details Strength 12.5 mg Package Details 100 Tablets/Bottle NDC number 57844-0112-01 View PI Product Details Strength 15 mg Package Details 100 Tablets/Bottle NDC number 57844-0115-01 View PI Product DetailsNDC:16714-130-01. Triamcinolone acetonide injectable suspension USP, 40 mg per mL. Rx Only Northstar Rx LLC. Carton Label . PRINCIPAL DISPLAY PANEL. NDC:16714-130-25.National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Apr 20, 2022 · Pharmacokinetics. Mixed Salts of a Single Entity Amphetamine Product contain d-amphetamine and l-amphetamine salts in the ratio of 3:1. Following administration of a single dose 10 or 30 mg of Mixed Salts of a Single Entity Amphetamine Product to healthy volunteers under fasted conditions, peak plasma concentrations occurred approximately 3 hours post-dose for both d-amphetamine and l-amphetamine. NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...Jan 12, 2022 · ORAL TABS 57844-130-01 30 each 338.25 ... Medication NDC 30 Day Supply Quantity Unit 30 Day Supply Cash Price BACLOFEN 10 MG ORAL TABS 0172-4096-60 30 each 89.82 NDC 57844-130-01 100 TABLET in 1 BOTTLE (57844-130-01) Marketing Start Date: 2014-02-06: NDC Exclude Flag: N: Sample Package? N: NDC SPL Data Element Entries.Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug ApplicationMar 10, 2022 · 3/10/2022 Amphetamine Mixed Salts, Immediate-Release Tablets Products Affected - Description Amphetamine mixed salts immediate release tablet, Mylan, 12.5 mg, bottle, 100 count, NDC 00378-4544-01 - discontinued Amphetamine mixed salts immediate release tablet, Mylan, 15 mg, bottle, 100 count, NDC 00378-4545-01 - discontinued in a 10-digit format. Proper billing of a National Drug Code (NDC) requires an 11-digit number in a 5-4-2 format. Converting National Drug Code (NDC) from a 10-digit to an 11-digit format requires a strategically placed zero, dependent upon the 10-digit format. The following table shows common 10-digit National Drug Code (NDC) formatsThe National Drug Code (NDC) Directory is updated daily. Current through: 8/30/2023. NDC Application Programming Interface (API) (Firefox and Chrome recommended) Finished Products Unfinished Products Compounded Products.National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01).Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01).Generic Name,Company Name, Contact Info, Presentation, Type of Update,Date of Update, Availability Information, Related Information, Resolved Note, Reason for ... Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01).Product Details Strength 12.5 mg Package Details 100 Tablets/Bottle NDC number 57844-0112-01 View PI Product Details Strength 15 mg Package Details 100 Tablets/Bottle NDC number 57844-0115-01 View PI Product Detailsin a 10-digit format. Proper billing of a National Drug Code (NDC) requires an 11-digit number in a 5-4-2 format. Converting National Drug Code (NDC) from a 10-digit to an 11-digit format requires a strategically placed zero, dependent upon the 10-digit format. The following table shows common 10-digit National Drug Code (NDC) formatsNDC Number: 57844-0181-13: Product Dating: McKesson Acceptable Dating: we will ship >= 180 days: Storage Requirements: USP Controlled Room Temperature: Strength: 10 ...Skip to Main Content; National Library of Medicine. National Library of MedicineDec 28, 2022 · NDC:16714-130-01. Triamcinolone acetonide injectable suspension USP, 40 mg per mL. Rx Only Northstar Rx LLC. Carton Label . PRINCIPAL DISPLAY PANEL. NDC:16714-130-25. They are available in bottles of 100 tablets (NDC 57844-130-01). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).Generic Name,Company Name, Contact Info, Presentation, Type of Update,Date of Update, Availability Information, Related Information, Resolved Note, Reason for ...Adderall ® CII (Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product)) Rx only May 30, 2023 · NDC 57844-105-01. Adderall ® CII ... NDC:57844-130-01: 100 TABLET in 1 BOTTLE: None: Marketing Information: Marketing Category: Application Number or Monograph Citation: Nov 9, 2022 · 1000 Tablets NDC 11534-190-03. 7.5 mg: Blue, round tablets, debossed “N30” on one side and quadrisect on the other side having functional score. They are available in bottles of. 100 Tablets Unit-of-use NDC 11534-191-01 National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... The product is distributed in a single package with assigned NDC code 57844-130-01 100 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk. Jan 12, 2022 · ORAL TABS 57844-130-01 30 each 338.25 ... Medication NDC 30 Day Supply Quantity Unit 30 Day Supply Cash Price BACLOFEN 10 MG ORAL TABS 0172-4096-60 30 each 89.82 Product Details Strength 12.5 mg Package Details 100 Tablets/Bottle NDC number 57844-0112-01 View PI Product Details Strength 15 mg Package Details 100 Tablets/Bottle NDC number 57844-0115-01 View PI Product Details National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Bottles of 100….NDC 0406-8891-01 7.5 mg: White to cream colored/mottled pillow shaped tablet, debossed with a “7.5” and a partial quadrisect on one side and a on the other side. Bottles of 100….NDC 0406-8884-01National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... In addition, Janssen CarePath can also investigate specialty pharmacies that may be available to simplify product procurement and billing for healthcare providers. If you have any questions, please call a Janssen CarePath Care Coordinator at 877-CarePath (877-227-3728), Monday-Friday, 8:00 AM to 8:00 PM ET.Aug 28, 2023 · Triamcinolone acetonide injectable suspension, USP is a synthetic glucocorticoid corticosteroid with anti-inflammatory action. THIS FORMULATION IS SUITABLE FOR INTRAMUSCULAR AND INTRA-ARTICULAR USE ONLY. THIS FORMULATION IS NOT FOR INTRADERMAL INJECTION. Each mL of the sterile aqueous suspension provides 40 mg triamcinolone acetonide, with 0.66 ... Requests for more specific information should be submitted in writing or directed to FDA's Freedom of Information Staff at: Food and Drug Administration. Freedom of Information Office, New ...Generic Name,Company Name, Contact Info, Presentation, Type of Update,Date of Update, Availability Information, Related Information, Resolved Note, Reason for ...100 tablets Unit of use NDC 72516-011-01 Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...The NDC Packaged Code 57844-130-01 is assigned to a package of 100 tablet in 1 bottle of Adderall, a human prescription drug labeled by Teva Pharmaceuticals Usa, Inc.. The product's dosage form is tablet and is administered via oral form. Is NDC 57844-130 included in the NDC Directory?NDC 47426-201-01 Rx Only. CINVANTI ® (aprepitant) injectable emulsion. 130 mg/18 mL (7.2 mg/mL) For Intravenous Use Only. Must be refrigerated. Store at 2°C-8°C (36°F-46°F). Do Not Freeze. 1 Sterile Single-Dose Vial Discard Unused Portion. Not For Sale. HERON THERAPEUTICSNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Jun 30, 2023 · NP Thyroid oral tablet, Acella, 120 mg bottle, 100 count, NDC 42192-0328-01 NP Thyroid oral tablet, Acella, 15 mg bottle, 100 count, NDC 42192-0327-01 Estimated Resupply Dates National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...13. Where do I enter NDC data on electronic claim (ANSI 5010 837P. or ANSI 5010 837I) transactions? Here are general guidelines for including NDC data in an electronic claim: Field Name Field Description Loop ID Segment . Product ID Qualifier Enter . N4. in this field 2410 LIN02 National Drug Code Enter the 11-digit NDC billing formatFeb 26, 2020 · NDC 42494-416-25. CIV PHENOBARBITAL Sodium Injection, USP. 130 mg/mL R x only. FOR IM OR SLOW IV USE. 25 x 1 mL Vials. Store at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature] DO NOT USE IF DISCOLORED OR CONTAINS A PRECIPITATE. MANUFACTURED FOR: CAMERON PHARMACEUTICALS LLC. GTIN: 00342494416258 SN: 115000433564 EXP: 01-2030 LOT ... Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01.Mar 10, 2022 · 3/10/2022 Amphetamine Mixed Salts, Immediate-Release Tablets Products Affected - Description Amphetamine mixed salts immediate release tablet, Mylan, 12.5 mg, bottle, 100 count, NDC 00378-4544-01 - discontinued Amphetamine mixed salts immediate release tablet, Mylan, 15 mg, bottle, 100 count, NDC 00378-4545-01 - discontinued Adderall immediate release tablet, Teva, 5 mg, bottle, 100 count, NDC 57844-0105-01 Adderall immediate release tablet, Teva, 7.5 mg, bottle, 100 count, NDC 57844-0117-01 Amphetamine mixed salts immediate release tablet, Mallinckrodt, 10 mg, bottle, 100 count, NDC 00406-8892-0190696 130: ProQuad (VFC) MMRV: 12 months - 12 years 0.5 ml: SC ... NDC: 42515-001-01 90738 134. JE-VAX - Japanese Encephalitis Japanese Encephalitis. 12 months ... NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...Product Details Strength 12.5 mg Package Details 100 Tablets/Bottle NDC number 57844-0112-01 View PI Product Details Strength 15 mg Package Details 100 Tablets/Bottle NDC number 57844-0115-01 View PI Product DetailsNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... SEARCH RESULTS for: 7CVR7L4A2D (1000 results) Only the first 1000 of 3471 Advanced Search results were returned, please refine your search further by modifying your query. The National Drug Code (NDC) Directory is updated daily. Current through: 8/30/2023. NDC Application Programming Interface (API) (Firefox and Chrome recommended) Finished Products Unfinished Products Compounded Products.Adderall ® CII (Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product)) Rx only National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01.NDC: Methylprednisolone Sodium Succinate for Injection, USP: Packaging Configuration: NDC 43598-127-25: 40 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-129-25: 125 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-128-11 : 500 mg Multi-Dose Vial: 1 vial per Carton: NDC 43598-130-74: 1 g Multi-Dose Vial: 1 vial per CartonTriamcinolone acetonide injectable suspension, USP is a synthetic glucocorticoid corticosteroid with anti-inflammatory action. THIS FORMULATION IS SUITABLE FOR INTRAMUSCULAR AND INTRA-ARTICULAR USE ONLY. THIS FORMULATION IS NOT FOR INTRADERMAL INJECTION. Each mL of the sterile aqueous suspension provides 40 mg triamcinolone acetonide, with 0.66 ...NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug Application 57844-117-01, 57844-120-01, 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine sulfate and amphetamine aspartate) capsule, extended release National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...

Jun 30, 2023 · NP Thyroid oral tablet, Acella, 120 mg bottle, 100 count, NDC 42192-0328-01 NP Thyroid oral tablet, Acella, 15 mg bottle, 100 count, NDC 42192-0327-01 Estimated Resupply Dates . Hitler

ndc 57844 130 01

ADDERALL (dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate) tablet. ... view full title. NDC Code (s): 57844-105-01, 57844-110-01, 57844-112-01, 57844-115-01, view more. 57844-117-01, 57844-120-01, 57844-130-01. Packager: Teva Pharmaceuticals USA, Inc.Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01). National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...in a 10-digit format. Proper billing of a National Drug Code (NDC) requires an 11-digit number in a 5-4-2 format. Converting National Drug Code (NDC) from a 10-digit to an 11-digit format requires a strategically placed zero, dependent upon the 10-digit format. The following table shows common 10-digit National Drug Code (NDC) formatsThe product is distributed in a single package with assigned NDC code 57844-130-01 100 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk. Manufacturer/ NDC Number CPT Code: CVX Code Quadracel™ VFC: DTaP/IPV 4 - 6 years: 0.5 ml IM: Sanofi Pasteur – PMC NDC: 49281-0562-10 (1 dose vial) 90696 130: Kinrix® VFC: DTaP/IPV 4 - 6 years: 0.5 ml IM: GlaxoSmithKline – SKB NDC: 58160-0812-11 (1 dose vial) NDC: 58160-0812-52 (1 dose T-L syringe) 90696: 130 Pediarix® VFC DTAP/HepB/IPV ...Requests for more specific information should be submitted in writing or directed to FDA's Freedom of Information Staff at: Food and Drug Administration. Freedom of Information Office, New ...MG. Zaltrap is available as 200 MG per 8 ML (25 MG per ML) solution, single-use vial, NDC 00024-5841-01. For this sample scenario: The NDC is 00024-5841-01 (the qualifier is N4) The unit of measure is ML The quantity (number of J-code units administered) is 400 The quantity (number of NDC units administered) is 16National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... Aug 28, 2023 · Triamcinolone acetonide injectable suspension, USP is a synthetic glucocorticoid corticosteroid with anti-inflammatory action. THIS FORMULATION IS SUITABLE FOR INTRAMUSCULAR AND INTRA-ARTICULAR USE ONLY. THIS FORMULATION IS NOT FOR INTRADERMAL INJECTION. Each mL of the sterile aqueous suspension provides 40 mg triamcinolone acetonide, with 0.66 ... segments of the NDC number, separated by hyphens per FDA website. o In the Open Payments application, this element corresponds to the “ National Drug Code (NDC) of Associated Covered Drug or Biological” field for PY2013 – PY2015 submissions or the “Associated Drug or Biological NDC” field for PY2016 onward submissions. • ProprietaryName National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01). Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01..

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