NDC 71335-0822

Naproxen Sodium

Naproxen Sodium

Naproxen Sodium is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Naproxen Sodium.

Product ID71335-0822_0e7697ad-25c6-4405-9f9b-791633cb1ef7
NDC71335-0822
Product TypeHuman Prescription Drug
Proprietary NameNaproxen Sodium
Generic NameNaproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-10-31
Marketing CategoryANDA / ANDA
Application NumberANDA200629
Labeler NameBryant Ranch Prepack
Substance NameNAPROXEN SODIUM
Active Ingredient Strength550 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 71335-0822-0

6 TABLET, FILM COATED in 1 BOTTLE (71335-0822-0)
Marketing Start Date2021-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0822-4 [71335082204]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-9 [71335082209]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-5 [71335082205]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-05-14

NDC 71335-0822-2 [71335082202]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-3 [71335082203]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-8 [71335082208]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-0 [71335082200]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-6 [71335082206]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-7 [71335082207]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

NDC 71335-0822-1 [71335082201]

Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200629
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-14

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM550 mg/1

OpenFDA Data

SPL SET ID:0e7697ad-25c6-4405-9f9b-791633cb1ef7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849431

    • 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 "Naproxen Sodium" or generic name "Naproxen Sodium"

    NDCBrand NameGeneric Name
    68016-056Naproxen SodiumNaproxen Sodium
    68016-661Naproxen SodiumNaproxen Sodium
    68016-660Naproxen SodiumNaproxen Sodium
    68071-3054Naproxen SodiumNaproxen Sodium
    68071-3223Naproxen SodiumNaproxen Sodium
    68210-0040NAPROXEN SODIUMNAPROXEN SODIUM
    68210-0400NAPROXEN SODIUMNAPROXEN SODIUM
    68387-545Naproxen SodiumNaproxen Sodium
    68462-179Naproxen SodiumNaproxen Sodium
    68462-178Naproxen SodiumNaproxen Sodium
    68788-6406Naproxen SodiumNaproxen Sodium
    68788-7304Naproxen SodiumNaproxen Sodium
    68788-6934Naproxen SodiumNaproxen Sodium
    68788-7367Naproxen SodiumNaproxen Sodium
    68788-9022Naproxen SodiumNaproxen Sodium
    68998-144NAPROXEN SODIUMNAPROXEN SODIUM
    68998-145NAPROXEN SODIUMNAPROXEN SODIUM
    69168-632Naproxen SodiumNaproxen Sodium
    69230-305Naproxen SodiumNaproxen Sodium
    69452-179Naproxen SodiumNaproxen Sodium
    69469-169Naproxen SodiumNaproxen Sodium
    69842-010naproxen sodiumnaproxen sodium
    69842-748Naproxen SodiumNaproxen Sodium
    69842-417Naproxen SodiumNaproxen Sodium
    69842-975Naproxen SodiumNaproxen Sodium
    69842-811Naproxen SodiumNaproxen Sodium
    70518-0409Naproxen SodiumNaproxen Sodium
    70518-0178Naproxen sodiumNaproxen sodium
    70518-0724Naproxen SodiumNaproxen Sodium
    70518-1172Naproxen SodiumNaproxen Sodium
    71141-116NAPROXEN SODIUMNAPROXEN SODIUM
    71141-008Naproxen SodiumNaproxen Sodium
    71335-0274Naproxen SodiumNaproxen Sodium
    71335-0822Naproxen SodiumNaproxen Sodium
    71335-1061Naproxen SodiumNaproxen Sodium
    10544-275Naproxen SodiumNaproxen Sodium
    10544-128Naproxen SodiumNaproxen Sodium
    10544-063Naproxen SodiumNaproxen Sodium
    10544-276Naproxen SodiumNaproxen Sodium
    11673-175Naproxen SodiumNaproxen Sodium
    11822-0507naproxen sodiumnaproxen sodium
    11673-748Naproxen SodiumNaproxen Sodium
    11822-0490naproxen sodiumnaproxen sodium
    11822-0140Naproxen SodiumNaproxen Sodium
    21130-174Naproxen SodiumNaproxen Sodium
    21130-748Naproxen SodiumNaproxen Sodium
    21695-090Naproxen SodiumNaproxen Sodium
    17856-0194Naproxen SodiumNaproxen Sodium
    25000-141Naproxen SodiumNaproxen Sodium
    25000-144Naproxen SodiumNaproxen Sodium
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