Nabumetone - 49999-102-20 - (Nabumetone)

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Drug Information of Nabumetone

Product NDC: 49999-102
Proprietary Name: Nabumetone
Non Proprietary Name: Nabumetone
Active Ingredient(s): 500    mg/1 & nbsp;   Nabumetone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Nabumetone

Product NDC: 49999-102
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075280
Marketing Category: ANDA
Start Marketing Date: 20100826

Package Information of Nabumetone

Package NDC: 49999-102-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-102-20)

NDC Information of Nabumetone

NDC Code 49999-102-20
Proprietary Name Nabumetone
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-102-20)
Product NDC 49999-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100826
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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