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Topcare All Day Pain Relief - 36800-490-76 - (Naproxen Sodium)

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Drug Information of Topcare All Day Pain Relief

Product NDC: 36800-490
Proprietary Name: Topcare 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 Topcare All Day Pain Relief

Product NDC: 36800-490
Labeler Name: Topco Associates LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970114

Package Information of Topcare All Day Pain Relief

Package NDC: 36800-490-76
Package Description: 1 BOTTLE in 1 CARTON (36800-490-76) > 120 TABLET in 1 BOTTLE

NDC Information of Topcare All Day Pain Relief

NDC Code 36800-490-76
Proprietary Name Topcare All Day Pain Relief
Package Description 1 BOTTLE in 1 CARTON (36800-490-76) > 120 TABLET in 1 BOTTLE
Product NDC 36800-490
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970114
Marketing Category Name ANDA
Labeler Name Topco Associates LLC
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Topcare All Day Pain Relief


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