Nabumetone - 49999-103-20 - (Nabumetone)

Alphabetical Index


Drug Information of Nabumetone

Product NDC: 49999-103
Proprietary Name: Nabumetone
Non Proprietary Name: Nabumetone
Active Ingredient(s): 750    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: 49999-103
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078671
Marketing Category: ANDA
Start Marketing Date: 20101116

Package Information of Nabumetone

Package NDC: 49999-103-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-103-20)

NDC Information of Nabumetone

NDC Code 49999-103-20
Proprietary Name Nabumetone
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-103-20)
Product NDC 49999-103
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101116
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name NABUMETONE
Strength Number 750
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