25000-087 : Famotidine 20 mg 20 mg 20 mg Oral Tablet, Coated


NDC: 25000-087
Labeler: Marksans Pharma Limited
Product Type: Human OTC Drug
Drug Name:  Famotidine 20 mg
Dosage Form: Oral Tablet, Coated
Application #: ANDA217543
Rev. Date: 


NDC Package Codes:

  • 25000-087-03: 1 BOTTLE IN 1 CARTON (25000‑087‑03) / 30 TABLET, COATED IN 1 BOTTLE
  • 25000-087-05: 1 BOTTLE IN 1 CARTON (25000‑087‑05) / 50 TABLET, COATED IN 1 BOTTLE
  • 25000-087-08: 1 BOTTLE IN 1 CARTON (25000‑087‑08) / 100 TABLET, COATED IN 1 BOTTLE
  • 25000-087-36: 3 BLISTER PACK IN 1 CARTON (25000‑087‑36) / 10 TABLET, COATED IN 1 BLISTER PACK
  • 25000-087-82: 1 BOTTLE IN 1 CARTON (25000‑087‑82) / 200 TABLET, COATED IN 1 BOTTLE

Active Ingredients:

  • Famotidine

Dosage Strength:

  • 20 mg

Pharmaceutical Classes:

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

NDC QR Code

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NDC 25000-087 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.