NDC 72789-186 – Ibuprofen

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

Human Prescription Drug

Product NDC72789-186

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 (4)

Package NDCDescriptionSince
72789-186-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-30)May 18, 2021
72789-186-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-60)May 18, 2021
72789-186-82500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-82)May 11, 2021
72789-186-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-90)May 18, 2021

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