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"61919-668-30" National Drug Code (NDC)
Nabumetone 30 TABLET, FILM COATED in 1 BOTTLE (61919-668-30)
(Direct_Rx)
NDC Code
61919-668-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (61919-668-30)
Product NDC
61919-668
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nabumetone
Non-Proprietary Name
Nabumetone
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190812
Marketing Category Name
ANDA
Application Number
ANDA078671
Manufacturer
Direct_Rx
Substance Name
NABUMETONE
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-668-30