NDC 11822-0050 – Ibuprofen pm

Diphenhydramine Citrate 38 mg/1; Ibuprofen 200 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC11822-0050

Product details

Brand name
Ibuprofen pm
Generic name
Diphenhydramine Citrate, Ibuprofen
Labeler
Rite Aid Corporation
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079113
Marketed since
March 19, 2009
Marketing end
October 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen PM →

Package NDC codes (1)

Package NDCDescriptionSince
11822-0050-31 BOTTLE in 1 CARTON (11822-0050-3) / 20 TABLET, FILM COATED in 1 BOTTLEMar 19, 2009

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