NDC 67877-739 – Ibuprofen

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

Human Prescription Drug

Product NDC67877-739

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214699
Marketed since
September 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (7)

Package NDCDescriptionSince
67877-739-01100 TABLET, FILM COATED in 1 BOTTLE (67877-739-01)Sep 15, 2026
67877-739-05500 TABLET, FILM COATED in 1 BOTTLE (67877-739-05)Sep 15, 2026
67877-739-3030 TABLET, FILM COATED in 1 BOTTLE (67877-739-30)Sep 15, 2026
67877-739-331 BLISTER PACK in 1 CARTON (67877-739-33) / 10 TABLET, FILM COATED in 1 BLISTER PACKSep 15, 2026
67877-739-5050 TABLET, FILM COATED in 1 BOTTLE (67877-739-50)Sep 15, 2026
67877-739-6060 TABLET, FILM COATED in 1 BOTTLE (67877-739-60)Sep 15, 2026
67877-739-9090 TABLET, FILM COATED in 1 BOTTLE (67877-739-90)Sep 15, 2026

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