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all day relief - 0904-5230-59 - (Naproxen Sodium)

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Drug Information of all day relief

Product NDC: 0904-5230
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of all day relief

Product NDC: 0904-5230
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970109

Package Information of all day relief

Package NDC: 0904-5230-59
Package Description: 1 BOTTLE in 1 CARTON (0904-5230-59) > 100 TABLET, FILM COATED in 1 BOTTLE

NDC Information of all day relief

NDC Code 0904-5230-59
Proprietary Name all day relief
Package Description 1 BOTTLE in 1 CARTON (0904-5230-59) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0904-5230
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970109
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of all day relief


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