NDC 85509-2396 – Ibuprofen

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

Human Prescription Drug

Product NDC85509-2396

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
PHOENIX RX LLC
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
85509-2396-330 TABLET, FILM COATED in 1 BOTTLE (85509-2396-3)Jul 30, 2025
85509-2396-660 TABLET, FILM COATED in 1 BOTTLE (85509-2396-6)Jul 30, 2025
85509-2396-990 TABLET, FILM COATED in 1 BOTTLE (85509-2396-9)Jul 30, 2025

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