Naproxen - 43063-092-06 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 43063-092
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 250    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 43063-092
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076494
Marketing Category: ANDA
Start Marketing Date: 20040114

Package Information of Naproxen

Package NDC: 43063-092-06
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC (43063-092-06)

NDC Information of Naproxen

NDC Code 43063-092-06
Proprietary Name Naproxen
Package Description 6 TABLET in 1 BOTTLE, PLASTIC (43063-092-06)
Product NDC 43063-092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040114
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name NAPROXEN
Strength Number 250
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