NDC 76282-714 – Ibuprofen

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

Human Prescription Drug

Product NDC76282-714

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
EXELAN PHARMACEUTICALS, INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091625
Marketed since
March 10, 2022
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (6)

Package NDCDescriptionSince
76282-714-10100 TABLET, FILM COATED in 1 BOTTLE (76282-714-10)Mar 10, 2022
76282-714-3030 TABLET, FILM COATED in 1 BOTTLE (76282-714-30)Mar 10, 2022
76282-714-46100 BLISTER PACK in 1 CARTON (76282-714-46) / 10 TABLET, FILM COATED in 1 BLISTER PACK (76282-714-45)Mar 10, 2022
76282-714-50500 TABLET, FILM COATED in 1 BOTTLE (76282-714-50)Mar 10, 2022
76282-714-551000 TABLET, FILM COATED in 1 BOTTLE (76282-714-55)Mar 10, 2022
76282-714-9090 TABLET, FILM COATED in 1 BOTTLE (76282-714-90)Mar 10, 2022

Other Ibuprofen products