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Leader All Day Pain Relief - 37205-261-78 - (Naproxen Sodium)

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Drug Information of Leader All Day Pain Relief

Product NDC: 37205-261
Proprietary Name: Leader 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 Leader All Day Pain Relief

Product NDC: 37205-261
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20010926

Package Information of Leader All Day Pain Relief

Package NDC: 37205-261-78
Package Description: 1 BOTTLE in 1 BOX (37205-261-78) > 100 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Leader All Day Pain Relief

NDC Code 37205-261-78
Proprietary Name Leader All Day Pain Relief
Package Description 1 BOTTLE in 1 BOX (37205-261-78) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC 37205-261
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20010926
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Leader All Day Pain Relief


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