NDC 49738-368

Smart Sense Naproxen Sodium

Naproxen Sodium

Smart Sense Naproxen Sodium is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Kmart Corporation. The primary component is Naproxen Sodium.

Product ID49738-368_c08ad15e-1c1b-45cd-a074-3926b5d67df6
NDC49738-368
Product TypeHuman Otc Drug
Proprietary NameSmart Sense Naproxen Sodium
Generic NameNaproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2010-10-08
Marketing CategoryANDA / ANDA
Application NumberANDA074661
Labeler NameKmart Corporation
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49738-368-90

500 TABLET, FILM COATED in 1 BOTTLE (49738-368-90)
Marketing Start Date2013-08-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49738-368-76 [49738036876]

Smart Sense Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-08-30

NDC 49738-368-90 [49738036890]

Smart Sense Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-08-30

NDC 49738-368-82 [49738036882]

Smart Sense Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-19

NDC 49738-368-71 [49738036871]

Smart Sense Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-10-08

NDC 49738-368-62 [49738036862]

Smart Sense Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-10-08

NDC 49738-368-78 [49738036878]

Smart Sense Naproxen Sodium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA074661
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-03

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:0ca47a22-654d-4b30-ba77-8494e708b07e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574

    • NDC Crossover Matching brand name "Smart Sense Naproxen Sodium" or generic name "Naproxen Sodium"

    NDCBrand NameGeneric Name
    49738-368Smart Sense Naproxen SodiumSmart Sense Naproxen Sodium
    49738-490Smart Sense naproxen sodiumSmart Sense naproxen sodium
    49738-140smart sense naproxen sodiumsmart sense naproxen sodium
    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.