Naproxen - 65862-522-01 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 65862-522
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: 65862-522
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200429
Marketing Category: ANDA
Start Marketing Date: 20111108

Package Information of Naproxen

Package NDC: 65862-522-01
Package Description: 100 TABLET in 1 BOTTLE (65862-522-01)

NDC Information of Naproxen

NDC Code 65862-522-01
Proprietary Name Naproxen
Package Description 100 TABLET in 1 BOTTLE (65862-522-01)
Product NDC 65862-522
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111108
Marketing Category Name ANDA
Labeler Name Aurobindo 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