Naproxen - 0093-0149-10 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 0093-0149
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: 0093-0149
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074201
Marketing Category: ANDA
Start Marketing Date: 19931222

Package Information of Naproxen

Package NDC: 0093-0149-10
Package Description: 1000 TABLET in 1 BOTTLE (0093-0149-10)

NDC Information of Naproxen

NDC Code 0093-0149-10
Proprietary Name Naproxen
Package Description 1000 TABLET in 1 BOTTLE (0093-0149-10)
Product NDC 0093-0149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19931222
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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