NDC 72789-212 – Ibuprofen

Ibuprofen 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72789-212

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078329
Marketed since
August 21, 2020
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (9)

Package NDCDescriptionSince
72789-212-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-06)Aug 2, 2022
72789-212-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-10)Aug 2, 2022
72789-212-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-15)Oct 27, 2021
72789-212-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-20)Nov 19, 2021
72789-212-2121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-21)Aug 21, 2020
72789-212-2424 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-24)Oct 26, 2021
72789-212-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-30)Oct 19, 2021
72789-212-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-40)Jan 3, 2022
72789-212-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-212-90)Oct 25, 2021

Other Ibuprofen products