United States · FDA National Drug Code directory
Ibuprofen
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
- 68016-634_4ce3d600-a2ba-4e98-b513-e6e5884ae9a2
- Product NDC
- 68016-634
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Chain Drug Consortium
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19880524 / 20270228
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68016-634-00) · 68016-634-00
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68016-634-05) · 68016-634-05
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-634-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 68016-634-10
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-634-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 68016-634-24
- 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68016-634-25) · 68016-634-25
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-634-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 68016-634-50
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 →