Home > National Drug Code (NDC) > Naproxen Sodium

Naproxen Sodium - 68462-179-01 - (Naproxen Sodium)

Alphabetical Index


Drug Information of Naproxen Sodium

Product NDC: 68462-179
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 550    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Sodium

Product NDC: 68462-179
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078314
Marketing Category: ANDA
Start Marketing Date: 20070801

Package Information of Naproxen Sodium

Package NDC: 68462-179-01
Package Description: 100 TABLET in 1 BOTTLE (68462-179-01)

NDC Information of Naproxen Sodium

NDC Code 68462-179-01
Proprietary Name Naproxen Sodium
Package Description 100 TABLET in 1 BOTTLE (68462-179-01)
Product NDC 68462-179
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070801
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
Substance Name NAPROXEN SODIUM
Strength Number 550
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen Sodium


General Information