NDC 55289-453

Daypro

Oxaprozin

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

• Product ID: 55289-453_7c1fbf8f-0192-264c-e053-2991aa0a678f
• NDC: 55289-453
• Product Type: Human Prescription Drug
• Proprietary Name: Daypro
• Generic Name: Oxaprozin
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1992-10-29
• Marketing Category: NDA / NDA
• Application Number: NDA018841
• Labeler Name: PD-Rx Pharmaceuticals, Inc.
• Substance Name: OXAPROZIN
• Active Ingredient Strength: 600 mg/1
• Pharm Classes: Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55289-453-14

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-453-14)

• Marketing Start Date: 2010-04-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55289-453-40 [55289045340]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

NDC 55289-453-20 [55289045320]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

NDC 55289-453-42 [55289045342]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

NDC 55289-453-30 [55289045330]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

NDC 55289-453-14 [55289045314]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

NDC 55289-453-15 [55289045315]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

NDC 55289-453-60 [55289045360]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-04-14

Drug Details

Active Ingredients

Ingredient	Strength
OXAPROZIN	600 mg/1

OpenFDA Data

• SPL SET ID: 755ca241-0d01-41ba-a735-e37365352a71
• Manufacturer:
  • PD-Rx Pharmaceuticals, Inc.
• UNII:
  • MHJ80W9LRB
• RxNorm Concept Unique ID - RxCUI:
  • 207243
  • 312132
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• UPC Code:
  • 0355289453307
• 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 "Daypro" or generic name "Oxaprozin"

NDC	Brand Name	Generic Name
0025-1381	Daypro	oxaprozin
55289-453	Daypro	oxaprozin
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