Nabumetone - 49884-650-05 - (Nabumetone)

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Drug Information of Nabumetone

Product NDC: 49884-650
Proprietary Name: Nabumetone
Non Proprietary Name: Nabumetone
Active Ingredient(s): 750    mg/1 & nbsp;   Nabumetone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nabumetone

Product NDC: 49884-650
Labeler Name: Par Pharmaceutical Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076009
Marketing Category: ANDA
Start Marketing Date: 20030124

Package Information of Nabumetone

Package NDC: 49884-650-05
Package Description: 500 TABLET in 1 BOTTLE (49884-650-05)

NDC Information of Nabumetone

NDC Code 49884-650-05
Proprietary Name Nabumetone
Package Description 500 TABLET in 1 BOTTLE (49884-650-05)
Product NDC 49884-650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030124
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc
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