United States · FDA National Drug Code directory
Ibuprofen and 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
- 69306-266_57ff667b-550b-d328-e063-6294a90a5073
- Product NDC
- 69306-266
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen and famotidine
- Labeler
- Doc Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210804
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
- FAMOTIDINE — 26.6 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (69306-266-30) · 69306-266-30
- 60 TABLET, FILM COATED in 1 BOTTLE (69306-266-60) · 69306-266-60
- 90 TABLET, FILM COATED in 1 BOTTLE (69306-266-90) · 69306-266-90
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 →