Nabumetone - 10544-273-40 - (Nabumetone)

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Drug Information of Nabumetone

Product NDC: 10544-273
Proprietary Name: Nabumetone
Non Proprietary Name: Nabumetone
Active Ingredient(s): 500    mg/1 & nbsp;   Nabumetone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nabumetone

Product NDC: 10544-273
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076009
Marketing Category: ANDA
Start Marketing Date: 20100324

Package Information of Nabumetone

Package NDC: 10544-273-40
Package Description: 40 TABLET in 1 BOTTLE (10544-273-40)

NDC Information of Nabumetone

NDC Code 10544-273-40
Proprietary Name Nabumetone
Package Description 40 TABLET in 1 BOTTLE (10544-273-40)
Product NDC 10544-273
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100324
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, 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