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Being Well all day pain relief - 46994-368-71 - (Naproxen Sodium)

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Drug Information of Being Well all day pain relief

Product NDC: 46994-368
Proprietary Name: Being Well all day pain relief
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 220    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Being Well all day pain relief

Product NDC: 46994-368
Labeler Name: Save-A-Lot Food Stores Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20060225

Package Information of Being Well all day pain relief

Package NDC: 46994-368-71
Package Description: 1 BOTTLE in 1 CARTON (46994-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Being Well all day pain relief

NDC Code 46994-368-71
Proprietary Name Being Well all day pain relief
Package Description 1 BOTTLE in 1 CARTON (46994-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 46994-368
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060225
Marketing Category Name ANDA
Labeler Name Save-A-Lot Food Stores Ltd
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Being Well all day pain relief


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