NDC 72789-364 – Ibuprofen

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

Human Prescription Drug

Product NDC72789-364

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091625
Marketed since
December 21, 2015
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (10)

Package NDCDescriptionSince
72789-364-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-06)Mar 15, 2024
72789-364-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-10)Nov 13, 2023
72789-364-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-15)Dec 11, 2023
72789-364-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-20)Dec 11, 2023
72789-364-2121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-21)Dec 11, 2023
72789-364-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-30)Nov 14, 2023
72789-364-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-40)Nov 15, 2023
72789-364-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-60)Nov 13, 2023
72789-364-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-90)Nov 24, 2023
72789-364-93180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-93)Dec 12, 2023

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