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All Day Pain Relief - 0363-0368-61 - (Naproxen Sodium)

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Drug Information of All Day Pain Relief

Product NDC: 0363-0368
Proprietary Name: 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 All Day Pain Relief

Product NDC: 0363-0368
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970114

Package Information of All Day Pain Relief

Package NDC: 0363-0368-61
Package Description: 600 TABLET, FILM COATED in 1 BOTTLE (0363-0368-61)

NDC Information of All Day Pain Relief

NDC Code 0363-0368-61
Proprietary Name All Day Pain Relief
Package Description 600 TABLET, FILM COATED in 1 BOTTLE (0363-0368-61)
Product NDC 0363-0368
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970114
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of All Day Pain Relief


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