NDC 55289-601

Oxaprozin

Oxaprozin

Oxaprozin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, In. The primary component is Oxaprozin.

• Product ID: 55289-601_7c33b527-a03c-4895-e053-2a91aa0a91ca
• NDC: 55289-601
• 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: PD-Rx Pharmaceuticals, In
• Substance Name: OXAPROZIN
• Active Ingredient Strength: 600 mg/1
• Pharm Classes: Cyclooxygenase
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55289-601-20

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-601-20)

• Marketing Start Date: 2010-09-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55289-601-20 [55289060120]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-09-08

NDC 55289-601-60 [55289060160]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-09-08

NDC 55289-601-30 [55289060130]

Oxaprozin TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075849
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-09-08

Drug Details

Active Ingredients

Ingredient	Strength
OXAPROZIN	600 mg/1

OpenFDA Data

• SPL SET ID: 0920c0b1-a10a-4aec-8e92-4e35dedd383d
• Manufacturer:
  • PD-Rx Pharmaceuticals, Inc.
• UNII:
  • MHJ80W9LRB
• RxNorm Concept Unique ID - RxCUI:
  • 312132
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• UPC Code:
  • 0355289601203
• 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