NDC 57344-145

Naproxen Sodium

Naproxen Sodium

Naproxen Sodium is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Aaa Pharmaceutical, Inc.. The primary component is Naproxen Sodium.

Product ID57344-145_5d765fcc-bfa7-4791-b533-b28f73b01f40
NDC57344-145
Product TypeHuman Otc Drug
Proprietary NameNaproxen Sodium
Generic NameNaproxen Sodium
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2012-12-15
Marketing CategoryANDA / ANDA
Application NumberANDA079096
Labeler NameAAA Pharmaceutical, Inc.
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 57344-145-01

1 BOTTLE, PLASTIC in 1 CARTON (57344-145-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC
Marketing Start Date2012-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57344-145-05 [57344014505]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-02 [57344014502]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01

NDC 57344-145-01 [57344014501]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01

NDC 57344-145-08 [57344014508]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-11 [57344014511]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-10 [57344014510]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-07 [57344014507]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-03 [57344014503]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-06 [57344014506]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

NDC 57344-145-04 [57344014504]

Naproxen Sodium TABLET, COATED
Marketing CategoryANDA
Application NumberANDA079096
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-04-01
Marketing End Date2019-09-11

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:5ea3217d-845d-4781-b849-6b00babdc214
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574
  • 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

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