NDC 27854-170

AnaDent

Naproxen Sodium

AnaDent is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Belmora Llc. The primary component is Naproxen Sodium.

Product ID27854-170_11734bfe-845a-4c97-b140-02dba79649a6
NDC27854-170
Product TypeHuman Otc Drug
Proprietary NameAnaDent
Generic NameNaproxen Sodium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-01-23
Marketing CategoryANDA / ANDA
Application NumberANDA204872
Labeler NameBelmora LLC
Substance NameNAPROXEN SODIUM
Active Ingredient Strength220 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 27854-170-01

1 BOTTLE in 1 CARTON (27854-170-01) > 24 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2017-01-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 27854-170-01 [27854017001]

AnaDent TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204872
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-23

Drug Details

Active Ingredients

IngredientStrength
NAPROXEN SODIUM220 mg/1

OpenFDA Data

SPL SET ID:236674db-da4d-415c-a160-7086eaf5bff5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 849574
  • NDC Crossover Matching brand name "AnaDent" or generic name "Naproxen Sodium"

    NDCBrand NameGeneric Name
    27854-170AnaDentAnaDent
    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

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