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all day relief - 49614-142-71 - (Naproxen Sodium)

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Drug Information of all day relief

Product NDC: 49614-142
Proprietary Name: all day 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 all day relief

Product NDC: 49614-142
Labeler Name: Medicine Shoppe International Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20010903

Package Information of all day relief

Package NDC: 49614-142-71
Package Description: 1 BOTTLE in 1 CARTON (49614-142-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of all day relief

NDC Code 49614-142-71
Proprietary Name all day relief
Package Description 1 BOTTLE in 1 CARTON (49614-142-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 49614-142
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20010903
Marketing Category Name ANDA
Labeler Name Medicine Shoppe International Inc
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of all day relief


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