Nabumetone - 63874-687-30 - (Nabumetone)

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Drug Information of Nabumetone

Product NDC: 63874-687
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: 63874-687
Labeler Name: Altura Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076009
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Nabumetone

Package NDC: 63874-687-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (63874-687-30)

NDC Information of Nabumetone

NDC Code 63874-687-30
Proprietary Name Nabumetone
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (63874-687-30)
Product NDC 63874-687
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nabumetone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name Altura Pharmaceuticals, 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