NDC 72789-200 – Ibuprofen

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

Human Prescription Drug

Product NDC72789-200

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 (10)

Package NDCDescriptionSince
72789-200-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-10)Sep 28, 2021
72789-200-1212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-12)Oct 11, 2021
72789-200-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-15)Sep 21, 2021
72789-200-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-20)Sep 28, 2021
72789-200-2121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-21)Sep 28, 2021
72789-200-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-30)Aug 23, 2021
72789-200-4040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-40)Sep 28, 2021
72789-200-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-60)Aug 23, 2021
72789-200-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-90)Aug 23, 2021
72789-200-93180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-93)Sep 28, 2021

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