Naproxen - 31722-339-50 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 31722-339
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: 31722-339
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091432
Marketing Category: ANDA
Start Marketing Date: 20120123

Package Information of Naproxen

Package NDC: 31722-339-50
Package Description: 12 BOTTLE in 1 CASE (31722-339-50) > 500 TABLET in 1 BOTTLE (31722-339-10)

NDC Information of Naproxen

NDC Code 31722-339-50
Proprietary Name Naproxen
Package Description 12 BOTTLE in 1 CASE (31722-339-50) > 500 TABLET in 1 BOTTLE (31722-339-10)
Product NDC 31722-339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120123
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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