70518-4084 : Famotidine 40 mg Oral Tablet, Film Coated


NDC70518-4084
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Famotidine
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA215630
Rev. Date: 


NDC Package Codes:

  • 70518-4084-0: 30 TABLET, FILM COATED IN 1 BLISTER PACK (70518‑4084‑0)

Active Ingredients:

  • Famotidine

Dosage Strength:

  • 40 mg

Pharmaceutical Classes:

  • Histamine H2 Receptor Antagonists [MoA]
  • Histamine-2 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 70518-0163 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-0460 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-0461 Famotidine 20 mg Oral Tablet by Remedyrepack Inc.
  • 70518-1001 Famotidine 20 mg Oral Tablet by Remedyrepack Inc.
  • 70518-1089 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-1341 Famotidine 40 mg Oral Tablet by Remedyrepack Inc.
  • 70518-1415 Famotidine 40 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-1877 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-2469 Famotidine 20 mg Oral Tablet by Remedyrepack Inc.
  • 70518-3301 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-3829 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-3831 Famotidine 40 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-4077 Famotidine 40 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 49349-546 Famotidine 20 mg Oral Tablet by Remedyrepack Inc.
  • 49349-574 Famotidine 40 mg Oral Tablet by Remedyrepack Inc.
  • 49349-577 Famotidine 40 mg Oral Tablet by Remedyrepack Inc.
  • 52125-658 Famotidine 20 mg Oral Tablet by Remedyrepack Inc.
  • 61786-036 Famotidine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 61786-080 Famotidine 20 mg Oral Tablet by Remedyrepack Inc.
  • 61786-228 Famotidine 40 mg Oral Tablet by Remedyrepack Inc.
  • More related products ...

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.