Naproxen - 0093-1006-05 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 0093-1006
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 500    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 0093-1006
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075227
Marketing Category: ANDA
Start Marketing Date: 19980729

Package Information of Naproxen

Package NDC: 0093-1006-05
Package Description: 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-1006-05)

NDC Information of Naproxen

NDC Code 0093-1006-05
Proprietary Name Naproxen
Package Description 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-1006-05)
Product NDC 0093-1006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19980729
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