Nabumetone - 0185-0145-01 - (Nabumentone)

Alphabetical Index


Drug Information of Nabumetone

Product NDC: 0185-0145
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: 0185-0145
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075280
Marketing Category: ANDA
Start Marketing Date: 20020225

Package Information of Nabumetone

Package NDC: 0185-0145-01
Package Description: 100 TABLET in 1 BOTTLE (0185-0145-01)

NDC Information of Nabumetone

NDC Code 0185-0145-01
Proprietary Name Nabumetone
Package Description 100 TABLET in 1 BOTTLE (0185-0145-01)
Product NDC 0185-0145
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 Eon Labs, 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