Naproxen - 68462-188-01 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 68462-188
Proprietary Name: Naproxen
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 Naproxen

Product NDC: 68462-188
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078250
Marketing Category: ANDA
Start Marketing Date: 20070701

Package Information of Naproxen

Package NDC: 68462-188-01
Package Description: 100 TABLET in 1 BOTTLE (68462-188-01)

NDC Information of Naproxen

NDC Code 68462-188-01
Proprietary Name Naproxen
Package Description 100 TABLET in 1 BOTTLE (68462-188-01)
Product NDC 68462-188
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070701
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
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 Naproxen


General Information