NDC 37808-703 – Ibuprofen pm

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

Human Otc Drug

Product NDC37808-703

Product details

Brand name
Ibuprofen pm
Generic name
Diphenhydramine citrate, ibuprofen
Labeler
H E B
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079113
Marketed since
April 5, 2018
Listing expires
December 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
37808-703-601 BOTTLE in 1 CARTON (37808-703-60) / 20 TABLET, FILM COATED in 1 BOTTLEApr 5, 2018

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