NDC 50844-714

Naproxen Back and Muscle Pain

Naproxen Sodium

Naproxen Back and Muscle Pain is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by L.n.k. International, Inc.. The primary component is Naproxen Sodium.

Product ID50844-714_015d90ca-63cc-4300-828a-d3426f31766b
NDC50844-714
Product TypeHuman Otc Drug
Proprietary NameNaproxen Back and Muscle Pain
Generic NameNaproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-02-01
Marketing CategoryANDA / ANDA
Application NumberANDA204872
Labeler NameL.N.K. International, Inc.
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50844-714-14

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)
Marketing Start Date2019-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50844-714-98 [50844071498]

Naproxen Back and Muscle Pain TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-01

NDC 50844-714-14 [50844071414]

Naproxen Back and Muscle Pain TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-01

NDC 50844-714-99 [50844071499]

Naproxen Back and Muscle Pain TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-01

NDC 50844-714-56 [50844071456]

Naproxen Back and Muscle Pain TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-01

NDC 50844-714-19 [50844071419]

Naproxen Back and Muscle Pain TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-01

NDC 50844-714-16 [50844071416]

Naproxen Back and Muscle Pain TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-02-01

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:68944663-0dc0-4d3a-a36b-019061bdbfa0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574
    • UPC Code
  • 0350844714169

    • NDC Crossover Matching brand name "Naproxen Back and Muscle Pain" or generic name "Naproxen Sodium"

    NDCBrand NameGeneric Name
    50844-714Naproxen Back and Muscle PainNaproxen Back and Muscle Pain
    0280-6000AleveNAPROXEN SODIUM
    0280-6010AleveNAPROXEN SODIUM
    0280-6020AleveNAPROXEN SODIUM
    0280-0041Aleve Headache PainNaproxen Sodium
    0113-7033basic care naproxen sodiumNaproxen Sodium
    0113-7368Basic Care Naproxen SodiumNaproxen Sodium
    0113-7901basic care naproxen sodiumNaproxen Sodium
    0113-0901Good Sense Naproxen SodiumNaproxen Sodium
    0113-1412good sense naproxen sodiumnaproxen sodium
    0113-1773good sense naproxen sodiumNaproxen Sodium
    0113-4368Good Sense Naproxen SodiumNaproxen Sodium
    0280-0270MenstridolNAPROXEN SODIUM
    0143-9908NAPROXENnaproxen sodium
    0143-9916NAPROXENnaproxen sodium
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.