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: 37808-393_fb73f7f9-e6bc-4205-ba85-032ce0d551fc
Product NDC: 37808-393
Form: TABLET, FILM COATED
Composition / generic term: Ibuprofen
Labeler: H E B
Marketing category: ANDA
Marketing start / end (source format): 19990301
Source listing expiry: 20271231

Source-listed ingredients

IBUPROFEN — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE, PLASTIC in 1 CARTON (37808-393-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 37808-393-12
250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (37808-393-13) · 37808-393-13

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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