Drug Atlas

NDC 37808-922 – Ibuprofen

Ibuprofen 200 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC37808-922

Product details

Brand name: Ibuprofen
Generic name: Ibuprofen
Labeler: H E B
Dosage form: Tablet, Film Coated
Route: Oral
Marketing category: ANDA · ANDA075010
Marketed since: May 24, 1988
Listing expires: December 31, 2027
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

Active ingredients

Ibuprofen 200 mg/1

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (1)

Package NDC	Description	Since
37808-922-13	1 BOTTLE, PLASTIC in 1 CARTON (37808-922-13) / 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC	May 24, 1988

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