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 ID0025-1381_1d508849-28b8-4a9c-b850-fa47e2481fd5
NDC0025-1381
Product TypeHuman Prescription Drug
Proprietary NameDaypro
Generic NameOxaprozin
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1992-10-29
Marketing CategoryNDA / NDA
Application NumberNDA018841
Labeler NamePfizer Laboratories Div Pfizer Inc
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 0025-1381-31

100 TABLET, FILM COATED in 1 BOTTLE (0025-1381-31)
Marketing Start Date1992-10-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0025-1381-34 [00025138134]

Daypro TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA018841
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-10-29

NDC 0025-1381-31 [00025138131]

Daypro TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA018841
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1992-10-29

NDC 0025-1381-51 [00025138151]

Daypro TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA018841
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1992-10-29

Drug Details

Active Ingredients

IngredientStrength
OXAPROZIN600 mg/1

OpenFDA Data

SPL SET ID:ea1de47e-3101-4414-817c-0a098af8988c
Manufacturer
UNII
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"

    NDCBrand NameGeneric Name
    0025-1381Dayprooxaprozin
    55289-453Dayprooxaprozin
    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

    Trademark Results [Daypro]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    DAYPRO
    DAYPRO
    77822151 3866463 Dead/Cancelled
    KIMBERLY CLARK DE MEXICO, S.A.B. DE C.V.
    2009-09-08
    DAYPRO
    DAYPRO
    76220510 not registered Dead/Abandoned
    ARTICULOS HIGIENICOS, S.A. DE C.V.
    2001-03-06
    DAYPRO
    DAYPRO
    74559950 1949703 Dead/Cancelled
    G. D. Searle & Co.
    1994-08-11
    DAYPRO
    DAYPRO
    74559949 not registered Dead/Abandoned
    G. D. Searle & Co.
    1994-08-11
    DAYPRO
    DAYPRO
    74246755 1772191 Live/Registered
    G.D. SEARLE LLC
    1992-02-18

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