Drug Atlas

NDC 37808-709 – Ibuprofen

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

Human Otc Drug

Product NDC37808-709

Product details

Brand name: Ibuprofen
Generic name: Ibuprofen
Labeler: H E B
Dosage form: Tablet, Film Coated
Route: Oral
Marketing category: ANDA · ANDA077349
Marketed since: July 4, 2006
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
37808-709-71	1 BOTTLE in 1 CARTON (37808-709-71) / 50 TABLET, FILM COATED in 1 BOTTLE	Aug 21, 2006

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