NDC 63629-1836

Ketoprofen

Ketoprofen

Ketoprofen is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ketoprofen.

Product ID63629-1836_f0131449-7330-40f5-be8e-e536863c40e7
NDC63629-1836
Product TypeHuman Prescription Drug
Proprietary NameKetoprofen
Generic NameKetoprofen
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date1993-01-01
Marketing CategoryANDA / ANDA
Application NumberANDA073517
Labeler NameBryant Ranch Prepack
Substance NameKETOPROFEN
Active Ingredient Strength75 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63629-1836-6

24 CAPSULE in 1 BOTTLE (63629-1836-6)
Marketing Start Date1993-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-1836-4 [63629183604]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-9 [63629183609]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-06-13
Marketing End Date2017-12-31

NDC 63629-1836-8 [63629183608]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-06-13
Marketing End Date2017-12-31

NDC 63629-1836-1 [63629183601]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-3 [63629183603]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-5 [63629183605]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-6 [63629183606]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-7 [63629183607]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-2 [63629183602]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2017-12-31

NDC 63629-1836-0 [63629183600]

Ketoprofen CAPSULE
Marketing CategoryANDA
Application NumberANDA073517
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-06-13
Marketing End Date2017-12-31

Drug Details

Active Ingredients

IngredientStrength
KETOPROFEN75 mg/1

OpenFDA Data

SPL SET ID:ecf6bc02-233d-2c3b-1ba0-e5d708338e45
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197856
  • 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 "Ketoprofen" or generic name "Ketoprofen"

    NDCBrand NameGeneric Name
    0276-0504KetoprofenKetoprofen
    0276-0506KetoprofenKetoprofen
    0378-8200Ketoprofenketoprofen
    21695-340Ketoprofenketoprofen
    21695-341Ketoprofenketoprofen
    23155-020ketoprofenketoprofen
    23155-021ketoprofenketoprofen
    23155-022ketoprofenketoprofen
    33261-064KetoprofenKetoprofen
    42254-037KetoprofenKetoprofen
    43063-737KetoprofenKetoprofen
    45865-379KetoprofenKetoprofen
    45865-485KetoprofenKetoprofen
    50090-2729KetoprofenKetoprofen
    52959-245KetoprofenKetoprofen
    53217-221KetoprofenKetoprofen
    63187-018KetoprofenKetoprofen
    63629-1836KetoprofenKetoprofen
    63629-3642KetoprofenKetoprofen
    66267-126KetoprofenKetoprofen
    67296-0369KetoprofenKetoprofen
    68788-6400KetoprofenKetoprofen
    68788-9088KetoprofenKetoprofen
    69336-127KetoprofenKetoprofen

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.