Nabumetone - 52959-650-20 - (Nabumetone)

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Drug Information of Nabumetone

Product NDC: 52959-650
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: 52959-650
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078671
Marketing Category: ANDA
Start Marketing Date: 20080301

Package Information of Nabumetone

Package NDC: 52959-650-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (52959-650-20)

NDC Information of Nabumetone

NDC Code 52959-650-20
Proprietary Name Nabumetone
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (52959-650-20)
Product NDC 52959-650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080301
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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