Oxaprozin 55111-0170

Product NDC

55111-0170

Manufacturer: Dr. Reddy's Laboratories Limited
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 31, 2001
Listing Expires: December 31, 2027
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(2)

55111-0170-01

100 TABLET, FILM COATED in 1 BOTTLE (55111-170-01)

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55111-0170-05

500 TABLET, FILM COATED in 1 BOTTLE (55111-170-05)

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