NDC 72189-595 – Oxaprozin

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

Human Prescription Drug

Product NDC72189-595

Product details

Brand name
Oxaprozin
Generic name
Oxaprozin
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075855
Marketed since
December 2, 2024
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Oxaprozin →

Package NDC codes (1)

Package NDCDescriptionSince
72189-595-6060 TABLET, FILM COATED in 1 BOTTLE (72189-595-60)Dec 2, 2024

Other Oxaprozin products