Naproxen - 16590-163-82 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 16590-163
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: 16590-163
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074201
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Naproxen

Package NDC: 16590-163-82
Package Description: 180 TABLET in 1 BOTTLE (16590-163-82)

NDC Information of Naproxen

NDC Code 16590-163-82
Proprietary Name Naproxen
Package Description 180 TABLET in 1 BOTTLE (16590-163-82)
Product NDC 16590-163
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
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