NDC 71205-522 – Ibuprofen

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

Human Prescription Drug

Product NDC71205-522

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078329
Marketed since
August 24, 2018
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (6)

Package NDCDescriptionSince
71205-522-2020 TABLET, FILM COATED in 1 BOTTLE (71205-522-20)Jan 7, 2021
71205-522-2828 TABLET, FILM COATED in 1 BOTTLE (71205-522-28)Jan 7, 2021
71205-522-3030 TABLET, FILM COATED in 1 BOTTLE (71205-522-30)Jan 7, 2021
71205-522-4242 TABLET, FILM COATED in 1 BOTTLE (71205-522-42)Aug 1, 2024
71205-522-6060 TABLET, FILM COATED in 1 BOTTLE (71205-522-60)May 19, 2025
71205-522-9090 TABLET, FILM COATED in 1 BOTTLE (71205-522-90)May 19, 2025

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