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All Day Pain Relief - 59779-490-78 - (Naproxen Sodium)

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Drug Information of All Day Pain Relief

Product NDC: 59779-490
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
Coding System: National Drug Codes(NDC)

Labeler Information of All Day Pain Relief

Product NDC: 59779-490
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970123

Package Information of All Day Pain Relief

Package NDC: 59779-490-78
Package Description: 1 BOTTLE in 1 CARTON (59779-490-78) > 100 TABLET in 1 BOTTLE

NDC Information of All Day Pain Relief

NDC Code 59779-490-78
Proprietary Name All Day Pain Relief
Package Description 1 BOTTLE in 1 CARTON (59779-490-78) > 100 TABLET in 1 BOTTLE
Product NDC 59779-490
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970123
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of All Day Pain Relief


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