Naproxen - 42806-125-05 - (naproxen)

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Drug Information of Naproxen

Product NDC: 42806-125
Proprietary Name: Naproxen
Non Proprietary Name: naproxen
Active Ingredient(s): 375    mg/1 & nbsp;   naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 42806-125
Labeler Name: Epic Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091416
Marketing Category: ANDA
Start Marketing Date: 20120302

Package Information of Naproxen

Package NDC: 42806-125-05
Package Description: 500 TABLET in 1 BOTTLE (42806-125-05)

NDC Information of Naproxen

NDC Code 42806-125-05
Proprietary Name Naproxen
Package Description 500 TABLET in 1 BOTTLE (42806-125-05)
Product NDC 42806-125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120302
Marketing Category Name ANDA
Labeler Name Epic Pharma, LLC
Substance Name NAPROXEN
Strength Number 375
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