Oxaprozin 72189-0595

Product NDC

72189-0595

Manufacturer: Direct_rx
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 2, 2024
Listing Expires: December 31, 2026
Application: ANDA075855

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Active Ingredients

Ingredient	Strength
Oxaprozin	600 mg/1

Drug Class

Nonsteroidal Anti-inflammatory Drug [EPC]Anti-Inflammatory AgentsNon-Steroidal [CS]

Packaging Options(1)

72189-0595-60

60 TABLET, FILM COATED in 1 BOTTLE (72189-595-60)

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