NDC 72657-157 – Acetaminophen, Ibuprofen

Ibuprofen 125 mg/1; Acetaminophen 250 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug 1 recall

Product NDC72657-157

Product details

Brand name
Acetaminophen, Ibuprofen
Generic name
Acetaminophen, Ibuprofen
Labeler
GLENMARK THERAPEUTICS INC., USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA218311
Marketed since
May 7, 2024
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
72657-157-051 BOTTLE in 1 CARTON (72657-157-05) / 500 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024
72657-157-181 BOTTLE in 1 CARTON (72657-157-18) / 18 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024
72657-157-201 BOTTLE in 1 CARTON (72657-157-20) / 250 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024
72657-157-361 BOTTLE in 1 CARTON (72657-157-36) / 36 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024
72657-157-721 BOTTLE in 1 CARTON (72657-157-72) / 72 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024
72657-157-741 BOTTLE in 1 CARTON (72657-157-74) / 144 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024
72657-157-761 BOTTLE in 1 CARTON (72657-157-76) / 216 TABLET, FILM COATED in 1 BOTTLEMay 7, 2024

Recalls mentioning this NDC