NDC 49483-604 – Ibuprofen

Ibuprofen 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 4 recalls

Product NDC49483-604

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
TIME CAP LABORATORIES, INC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090796
Marketed since
December 30, 2015
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (4)

Package NDCDescriptionSince
49483-604-01100 TABLET, FILM COATED in 1 BOTTLE (49483-604-01)Dec 30, 2015
49483-604-0330 TABLET, FILM COATED in 1 BOTTLE (49483-604-03)Dec 30, 2015
49483-604-0550 TABLET, FILM COATED in 1 BOTTLE (49483-604-05)Dec 30, 2015
49483-604-50500 TABLET, FILM COATED in 1 BOTTLE (49483-604-50)Dec 30, 2015

Recalls mentioning this NDC

Other Ibuprofen products