NDC 71335-0307

Fenoprofen Calcium

Fenoprofen Calcium

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

Product ID71335-0307_209fdde4-6ab5-4b64-8d03-4a8078b76946
NDC71335-0307
Product TypeHuman Prescription Drug
Proprietary NameFenoprofen Calcium
Generic NameFenoprofen Calcium
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2016-05-19
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA017604
Labeler NameBryant Ranch Prepack
Substance NameFENOPROFEN CALCIUM
Active Ingredient Strength400 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 71335-0307-1

30 CAPSULE in 1 BOTTLE (71335-0307-1)
Marketing Start Date2022-02-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0307-2 [71335030702]

Fenoprofen Calcium CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA017604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-24

NDC 71335-0307-1 [71335030701]

Fenoprofen Calcium CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA017604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-24

NDC 71335-0307-3 [71335030703]

Fenoprofen Calcium CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA017604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-24

NDC 71335-0307-5 [71335030705]

Fenoprofen Calcium CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA017604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-24

NDC 71335-0307-4 [71335030704]

Fenoprofen Calcium CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA017604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-24

Drug Details

Active Ingredients

IngredientStrength
FENOPROFEN CALCIUM400 mg/1

OpenFDA Data

SPL SET ID:209fdde4-6ab5-4b64-8d03-4a8078b76946
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 858116

    • Pharmacological Class

    • Cyclooxygenase Inhibitors [MoA]
    • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
    • Nonsteroidal Anti-inflammatory Drug [EPC]
    • Anti-Inflammatory Agents
    • Non-Steroidal [CS]

    NDC Crossover Matching brand name "Fenoprofen Calcium" or generic name "Fenoprofen Calcium"

    NDCBrand NameGeneric Name
    0276-0501Fenoprofen CalciumFenoprofen Calcium
    0276-0502Fenoprofen CalciumFenoprofen Calcium
    0276-0503Fenoprofen CalciumFenoprofen Calcium
    0378-0471Fenoprofen CalciumFenoprofen Calcium
    15014-400Fenoprofen CalciumFenoprofen Calcium
    16571-688FENOPROFEN CALCIUMFENOPROFEN CALCIUM
    42195-100Fenoprofen Calciumfenoprofen calcium
    42195-471Fenoprofen CalciumFenoprofen Calcium
    50090-3572Fenoprofen Calciumfenoprofen calcium
    53217-169Fenoprofen Calciumfenoprofen calcium
    54288-131FENOPROFEN CALCIUMFENOPROFEN CALCIUM
    54288-132FENOPROFEN CALCIUMFENOPROFEN CALCIUM
    55289-334Fenoprofen CalciumFenoprofen Calcium
    63629-8016Fenoprofen Calciumfenoprofen calcium
    69101-400Fenoprofen CalciumFenoprofen Calcium
    69336-124FENOPROFEN CALCIUMFENOPROFEN CALCIUM
    71335-0307Fenoprofen CalciumFenoprofen Calcium
    62250-691FENOPROFENFENOPROFEN CALCIUM
    42195-308Nalfonfenoprofen calcium
    42195-600Nalfonfenoprofen calcium
    42195-688NALFONFenoprofen Calcium
    55700-853Nalfonfenoprofen calcium
    63187-706Nalfonfenoprofen calcium
    63629-7515Nalfonfenoprofen calcium
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.