Nabumetone - 68788-9908-1 - (Nabumetone)

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Drug Information of Nabumetone

Product NDC: 68788-9908
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: 68788-9908
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078671
Marketing Category: ANDA
Start Marketing Date: 20120130

Package Information of Nabumetone

Package NDC: 68788-9908-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (68788-9908-1)

NDC Information of Nabumetone

NDC Code 68788-9908-1
Proprietary Name Nabumetone
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (68788-9908-1)
Product NDC 68788-9908
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120130
Marketing Category Name ANDA
Labeler Name Preferred 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