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
- 68788-8897_e2f29ca9-9ec8-4b82-8c80-8628d9e3ab2f
- Product NDC
- 68788-8897
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen and famotidine
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250801
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
- FAMOTIDINE — 26.6 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-8897-9) · 68788-8897-9
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 →