Naproxen - 25000-140-03 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 25000-140
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: 25000-140
Labeler Name: MARKSANS PHARMA LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091416
Marketing Category: ANDA
Start Marketing Date: 20110228

Package Information of Naproxen

Package NDC: 25000-140-03
Package Description: 30 TABLET in 1 BOTTLE (25000-140-03)

NDC Information of Naproxen

NDC Code 25000-140-03
Proprietary Name Naproxen
Package Description 30 TABLET in 1 BOTTLE (25000-140-03)
Product NDC 25000-140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110228
Marketing Category Name ANDA
Labeler Name MARKSANS PHARMA LIMITED
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