Home > National Drug Code (NDC) > NAPROXEN SODIUM

NAPROXEN SODIUM - 42291-532-50 - (NAPROXEN SODIUM)

Alphabetical Index


Drug Information of NAPROXEN SODIUM

Product NDC: 42291-532
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: 42291-532
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078432
Marketing Category: ANDA
Start Marketing Date: 20070426

Package Information of NAPROXEN SODIUM

Package NDC: 42291-532-50
Package Description: 500 TABLET in 1 BOTTLE (42291-532-50)

NDC Information of NAPROXEN SODIUM

NDC Code 42291-532-50
Proprietary Name NAPROXEN SODIUM
Package Description 500 TABLET in 1 BOTTLE (42291-532-50)
Product NDC 42291-532
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NAPROXEN SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070426
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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