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
- 85766-222_5522df17-39cd-040b-e063-6394a90a5ae9
- Product NDC
- 85766-222
- Form
- TABLET, FILM COATED
- Composition / generic term
- Famotidine
- Labeler
- Sportpharm LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010416
- Source listing expiry
- 20271231
Source-listed ingredients
- FAMOTIDINE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (85766-222-01) · 85766-222-01
- 7 TABLET, FILM COATED in 1 BOTTLE (85766-222-07) · 85766-222-07
- 10 TABLET, FILM COATED in 1 BOTTLE (85766-222-10) · 85766-222-10
- 14 TABLET, FILM COATED in 1 BOTTLE (85766-222-14) · 85766-222-14
- 15 TABLET, FILM COATED in 1 BOTTLE (85766-222-15) · 85766-222-15
- 20 TABLET, FILM COATED in 1 BOTTLE (85766-222-20) · 85766-222-20
- 30 TABLET, FILM COATED in 1 BOTTLE (85766-222-30) · 85766-222-30
- 60 TABLET, FILM COATED in 1 BOTTLE (85766-222-60) · 85766-222-60
- 90 TABLET, FILM COATED in 1 BOTTLE (85766-222-90) · 85766-222-90
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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