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Good Sense All Day Pain Relief - 63629-1793-4 - (Naproxen Sodium)

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Drug Information of Good Sense All Day Pain Relief

Product NDC: 63629-1793
Proprietary Name: Good Sense 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 Good Sense All Day Pain Relief

Product NDC: 63629-1793
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079096
Marketing Category: ANDA
Start Marketing Date: 19970114

Package Information of Good Sense All Day Pain Relief

Package NDC: 63629-1793-4
Package Description: 40 TABLET, FILM COATED in 1 BOTTLE (63629-1793-4)

NDC Information of Good Sense All Day Pain Relief

NDC Code 63629-1793-4
Proprietary Name Good Sense All Day Pain Relief
Package Description 40 TABLET, FILM COATED in 1 BOTTLE (63629-1793-4)
Product NDC 63629-1793
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970114
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Good Sense All Day Pain Relief


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