NDC 11673-050 – up and up ibuprofen pm

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

Human Otc Drug

Product NDC11673-050

Product details

Brand name
up and up ibuprofen pm
Generic name
diphenhydramine citrate and ibuprofen
Labeler
Target Corporation
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079113
Marketed since
July 10, 2009
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for up and up ibuprofen pm →

Package NDC codes (3)

Package NDCDescriptionSince
11673-050-581 BOTTLE in 1 CARTON (11673-050-58) / 40 TABLET, FILM COATED in 1 BOTTLEJul 24, 2009
11673-050-601 BOTTLE in 1 CARTON (11673-050-60) / 20 TABLET, FILM COATED in 1 BOTTLEMar 10, 2026
11673-050-82200 TABLET, FILM COATED in 1 BOTTLE (11673-050-82)Jan 27, 2022