NDC 71921-181 – Ibuprofen

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

Human Prescription Drug

Product NDC71921-181

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA071268
Marketed since
October 21, 2021
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (2)

Package NDCDescriptionSince
71921-181-01100 TABLET, FILM COATED in 1 BOTTLE (71921-181-01)Oct 21, 2021
71921-181-50500 TABLET, FILM COATED in 1 BOTTLE (71921-181-50)Oct 21, 2021

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