United States · FDA National Drug Code directory

FAMOTIDINE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 80005-119_7753e6db-5fe8-4b35-8817-c50abda35144
Product NDC: 80005-119
Form: POWDER, FOR SUSPENSION
Composition / generic term: FAMOTIDINE
Labeler: Carnegie Pharmaceuticals LLC
Marketing category: ANDA
Marketing start / end (source format): 20230810
Source listing expiry: 20261231

Source-listed ingredients

FAMOTIDINE — 40 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

50 mL in 1 BOTTLE (80005-119-16) · 80005-119-16

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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