Naproxen - 0781-1653-01 - (Naproxen)

Alphabetical Index


Drug Information of Naproxen

Product NDC: 0781-1653
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 500    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 0781-1653
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075061
Marketing Category: ANDA
Start Marketing Date: 19980218

Package Information of Naproxen

Package NDC: 0781-1653-01
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0781-1653-01)

NDC Information of Naproxen

NDC Code 0781-1653-01
Proprietary Name Naproxen
Package Description 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0781-1653-01)
Product NDC 0781-1653
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19980218
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name NAPROXEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen


General Information