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All Day Pain Relief - 41163-169-50 - (Naproxen Sodium)

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Drug Information of All Day Pain Relief

Product NDC: 41163-169
Proprietary Name: 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
Coding System: National Drug Codes(NDC)

Labeler Information of All Day Pain Relief

Product NDC: 41163-169
Labeler Name: SuperValu (Equaline)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079096
Marketing Category: ANDA
Start Marketing Date: 20101115

Package Information of All Day Pain Relief

Package NDC: 41163-169-50
Package Description: 1 BOTTLE in 1 BOX (41163-169-50) > 50 TABLET in 1 BOTTLE

NDC Information of All Day Pain Relief

NDC Code 41163-169-50
Proprietary Name All Day Pain Relief
Package Description 1 BOTTLE in 1 BOX (41163-169-50) > 50 TABLET in 1 BOTTLE
Product NDC 41163-169
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name ANDA
Labeler Name SuperValu (Equaline)
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of All Day Pain Relief


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