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
- 42571-433_3b0aa4df-ee1f-e4e3-e063-6394a90a4c66
- Product NDC
- 42571-433
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- FAMOTIDINE
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231201
- 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 (42571-433-45) · 42571-433-45
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →