NDC 70010-068 – Ibuprofen

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

Human Prescription Drug

Product NDC70010-068

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091625
Marketed since
February 18, 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 (6)

Package NDCDescriptionSince
70010-068-01100 TABLET, FILM COATED in 1 BOTTLE (70010-068-01)Feb 18, 2026
70010-068-0330 TABLET, FILM COATED in 1 BOTTLE (70010-068-03)Feb 18, 2026
70010-068-05500 TABLET, FILM COATED in 1 BOTTLE (70010-068-05)Feb 18, 2026
70010-068-101000 TABLET, FILM COATED in 1 BOTTLE (70010-068-10)Feb 18, 2026
70010-068-5050 TABLET, FILM COATED in 1 BOTTLE (70010-068-50)Feb 18, 2026
70010-068-829 BLISTER PACK in 1 CARTON (70010-068-82) / 14 TABLET, FILM COATED in 1 BLISTER PACKFeb 18, 2026

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