NDC 68071-3778 – Ibuprofen

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

Human Prescription Drug

Product NDC68071-3778

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202413
Marketed since
May 23, 2024
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (3)

Package NDCDescriptionSince
68071-3778-220 TABLET, FILM COATED in 1 BOTTLE (68071-3778-2)Jan 29, 2025
68071-3778-330 TABLET, FILM COATED in 1 BOTTLE (68071-3778-3)Jan 21, 2025
68071-3778-550 TABLET, FILM COATED in 1 BOTTLE (68071-3778-5)May 21, 2025

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