NAPROXEN - 10544-111-20 - (NAPROXEN)

Alphabetical Index


Drug Information of NAPROXEN

Product NDC: 10544-111
Proprietary Name: NAPROXEN
Non Proprietary Name: NAPROXEN
Active Ingredient(s): 500    mg/1 & nbsp;   NAPROXEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of NAPROXEN

Product NDC: 10544-111
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091416
Marketing Category: ANDA
Start Marketing Date: 20130328

Package Information of NAPROXEN

Package NDC: 10544-111-20
Package Description: 20 TABLET in 1 BOTTLE (10544-111-20)

NDC Information of NAPROXEN

NDC Code 10544-111-20
Proprietary Name NAPROXEN
Package Description 20 TABLET in 1 BOTTLE (10544-111-20)
Product NDC 10544-111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NAPROXEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130328
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, 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