NDC 0025-1381

Daypro

Oxaprozin

Daypro is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Oxaprozin.

• Product ID: 0025-1381_1d508849-28b8-4a9c-b850-fa47e2481fd5
• NDC: 0025-1381
• 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: Pfizer Laboratories Div Pfizer Inc
• Substance Name: OXAPROZIN
• Active Ingredient Strength: 600 mg/1
• Pharm Classes: Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0025-1381-31

100 TABLET, FILM COATED in 1 BOTTLE (0025-1381-31)

• Marketing Start Date: 1992-10-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0025-1381-34 [00025138134]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1992-10-29

NDC 0025-1381-31 [00025138131]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1992-10-29

NDC 0025-1381-51 [00025138151]

Daypro TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA018841
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1992-10-29

Drug Details

Active Ingredients

Ingredient	Strength
OXAPROZIN	600 mg/1

OpenFDA Data

• SPL SET ID: ea1de47e-3101-4414-817c-0a098af8988c
• Manufacturer:
  • G.D. Searle LLC Division of Pfizer Inc
• UNII:
  • MHJ80W9LRB
• RxNorm Concept Unique ID - RxCUI:
  • 207243
  • 312132
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• UPC Code:
  • 0300251381317
• 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