NDC 60760-382

Oxaprozin

Oxaprozin

Oxaprozin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by St Mary's Medical Park Pharmacy. The primary component is Oxaprozin.

Product ID60760-382_e881db23-6527-c7d2-e053-2a95a90afc64
NDC60760-382
Product TypeHuman Prescription Drug
Proprietary NameOxaprozin
Generic NameOxaprozin
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-08-15
Marketing CategoryANDA /
Application NumberANDA075855
Labeler NameST MARY'S MEDICAL PARK PHARMACY
Substance NameOXAPROZIN
Active Ingredient Strength600 mg/1
Pharm ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 60760-382-14

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-382-14)
Marketing Start Date2022-08-15
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Oxaprozin" or generic name "Oxaprozin"

NDCBrand NameGeneric Name
0093-0924OxaprozinOxaprozin
0185-0141OxaprozinOxaprozin
21695-100OxaprozinOxaprozin
50090-2012OxaprozinOxaprozin
50436-2899OxaprozinOxaprozin
52959-800OxaprozinOxaprozin
55111-170OxaprozinOxaprozin
55289-601OxaprozinOxaprozin
57664-391OxaprozinOxaprozin
59762-6002oxaprozinoxaprozin
60760-092OxaprozinOxaprozin
60760-203OxaprozinOxaprozin
60760-382OxaprozinOxaprozin
61919-178OXAPROZINOXAPROZIN
61919-673OXAPROZINOXAPROZIN
62135-176OXAPROZINOXAPROZIN
68151-0523OxaprozinOxaprozin
69238-1120OxaprozinOxaprozin
70332-311OxaprozinOxaprozin
70332-310OXAPROZINOXAPROZIN
71335-0617OxaprozinOxaprozin
71335-0393OxaprozinOxaprozin
71335-0902OxaprozinOxaprozin
63629-1345OxaprozinOxaprozin
66336-722OxaprozinOxaprozin
72189-077OXAPROZINOXAPROZIN
0025-1381Dayprooxaprozin
55289-453Dayprooxaprozin
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.