NDC 72789-382 – Ibuprofen

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

Human Prescription Drug

Product NDC72789-382

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 (1)

Package NDCDescriptionSince
72789-382-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-382-30)Feb 21, 2024

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