Naprosyn - 63629-3202-4 - (Naproxen)

Alphabetical Index


Drug Information of Naprosyn

Product NDC: 63629-3202
Proprietary Name: Naprosyn
Non Proprietary Name: Naproxen
Active Ingredient(s): 250    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naprosyn

Product NDC: 63629-3202
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075927
Marketing Category: ANDA
Start Marketing Date: 20090901

Package Information of Naprosyn

Package NDC: 63629-3202-4
Package Description: 120 TABLET in 1 BOTTLE (63629-3202-4)

NDC Information of Naprosyn

NDC Code 63629-3202-4
Proprietary Name Naprosyn
Package Description 120 TABLET in 1 BOTTLE (63629-3202-4)
Product NDC 63629-3202
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090901
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name NAPROXEN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naprosyn


General Information