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all day relief - 52959-469-28 - (Naproxen Sodium)

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Drug Information of all day relief

Product NDC: 52959-469
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
Coding System: National Drug Codes(NDC)

Labeler Information of all day relief

Product NDC: 52959-469
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970109

Package Information of all day relief

Package NDC: 52959-469-28
Package Description: 28 TABLET in 1 BOTTLE (52959-469-28)

NDC Information of all day relief

NDC Code 52959-469-28
Proprietary Name all day relief
Package Description 28 TABLET in 1 BOTTLE (52959-469-28)
Product NDC 52959-469
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970109
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of all day relief


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