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all day relief - 42507-490-71 - (Naproxen Sodium)

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Drug Information of all day relief

Product NDC: 42507-490
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: 42507-490
Labeler Name: HyVee Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 19970401

Package Information of all day relief

Package NDC: 42507-490-71
Package Description: 1 BOTTLE in 1 CARTON (42507-490-71) > 50 TABLET in 1 BOTTLE

NDC Information of all day relief

NDC Code 42507-490-71
Proprietary Name all day relief
Package Description 1 BOTTLE in 1 CARTON (42507-490-71) > 50 TABLET in 1 BOTTLE
Product NDC 42507-490
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970401
Marketing Category Name ANDA
Labeler Name HyVee Inc
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of all day relief


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