NDC 63629-1345

Oxaprozin

Oxaprozin

Oxaprozin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Oxaprozin.

• Product ID: 63629-1345_14c85f63-ba26-4310-bdb6-7f4847ddea8b
• NDC: 63629-1345
• Product Type: Human Prescription Drug
• Proprietary Name: Oxaprozin
• Generic Name: Oxaprozin
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2003-05-12
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075849
• Labeler Name: Bryant Ranch Prepack
• Substance Name: OXAPROZIN
• Active Ingredient Strength: 600 mg/1
• Pharm Classes: Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 63629-1345-1

30 TABLET, FILM COATED in 1 BOTTLE (63629-1345-1)

• Marketing Start Date: 2009-12-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63629-1345-3 [63629134503]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-09

NDC 63629-1345-2 [63629134502]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-09

NDC 63629-1345-6 [63629134506]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2006-12-27

NDC 63629-1345-1 [63629134501]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-09

NDC 63629-1345-7 [63629134507]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2006-12-27

NDC 63629-1345-5 [63629134505]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-09

NDC 63629-1345-4 [63629134504]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-12-09

Drug Details

Active Ingredients

Ingredient	Strength
OXAPROZIN	600 mg/1

OpenFDA Data

• SPL SET ID: 765a0b09-d93b-eb04-7eed-1eb260500dc0
• Manufacturer:
  • Bryant Ranch Prepack
• UNII:
  • MHJ80W9LRB
• RxNorm Concept Unique ID - RxCUI:
  • 312132
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• NUI Code:
  • N0000000160
  • N0000175722
  • N0000175721

Pharmacological Class

• Cyclooxygenase Inhibitors [MoA]
• Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
• Nonsteroidal Anti-inflammatory Drug [EPC]

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

NDC	Brand Name	Generic Name
0093-0924	Oxaprozin	Oxaprozin
0185-0141	Oxaprozin	Oxaprozin
21695-100	Oxaprozin	Oxaprozin
50090-2012	Oxaprozin	Oxaprozin
50436-2899	Oxaprozin	Oxaprozin
52959-800	Oxaprozin	Oxaprozin
55111-170	Oxaprozin	Oxaprozin
55289-601	Oxaprozin	Oxaprozin
57664-391	Oxaprozin	Oxaprozin
59762-6002	oxaprozin	oxaprozin
60760-092	Oxaprozin	Oxaprozin
60760-203	Oxaprozin	Oxaprozin
60760-382	Oxaprozin	Oxaprozin
61919-178	OXAPROZIN	OXAPROZIN
61919-673	OXAPROZIN	OXAPROZIN
62135-176	OXAPROZIN	OXAPROZIN
68151-0523	Oxaprozin	Oxaprozin
69238-1120	Oxaprozin	Oxaprozin
70332-311	Oxaprozin	Oxaprozin
70332-310	OXAPROZIN	OXAPROZIN
71335-0617	Oxaprozin	Oxaprozin
71335-0393	Oxaprozin	Oxaprozin
71335-0902	Oxaprozin	Oxaprozin
63629-1345	Oxaprozin	Oxaprozin
66336-722	Oxaprozin	Oxaprozin
72189-077	OXAPROZIN	OXAPROZIN
0025-1381	Daypro	oxaprozin
55289-453	Daypro	oxaprozin