Nabumetone - 55289-611-60 - (Nabumentone)

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Drug Information of Nabumetone

Product NDC: 55289-611
Proprietary Name: Nabumetone
Non Proprietary Name: Nabumentone
Active Ingredient(s): 500    mg/1 & nbsp;   Nabumentone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nabumetone

Product NDC: 55289-611
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075280
Marketing Category: ANDA
Start Marketing Date: 20020225

Package Information of Nabumetone

Package NDC: 55289-611-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-611-60)

NDC Information of Nabumetone

NDC Code 55289-611-60
Proprietary Name Nabumetone
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-611-60)
Product NDC 55289-611
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumentone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020225
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name NABUMETONE
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 Nabumetone


General Information