NDC 43063-872 – Ibuprofen

Ibuprofen 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC43063-872

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
PD-Rx Pharmaceuticals, 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 (7)

Package NDCDescriptionSince
43063-872-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-06)Jan 25, 2019
43063-872-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-10)Apr 29, 2019
43063-872-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-20)Aug 7, 2018
43063-872-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-30)Aug 7, 2018
43063-872-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-40)Aug 7, 2018
43063-872-82500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-82)Mar 2, 2019
43063-872-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-872-90)Apr 26, 2019

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