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sunmark all day relief - 49348-819-09 - (Naproxen Sodium)

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Drug Information of sunmark all day relief

Product NDC: 49348-819
Proprietary Name: sunmark 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 sunmark all day relief

Product NDC: 49348-819
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20030811

Package Information of sunmark all day relief

Package NDC: 49348-819-09
Package Description: 1 BOTTLE in 1 CARTON (49348-819-09) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of sunmark all day relief

NDC Code 49348-819-09
Proprietary Name sunmark all day relief
Package Description 1 BOTTLE in 1 CARTON (49348-819-09) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 49348-819
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030811
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of sunmark all day relief


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