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"60687-630-21" National Drug Code (NDC)
Nabumetone 30 BLISTER PACK in 1 CARTON (60687-630-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-630-11)
(American Health Packaging)
NDC Code
60687-630-21
Package Description
30 BLISTER PACK in 1 CARTON (60687-630-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-630-11)
Product NDC
60687-630
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nabumetone
Non-Proprietary Name
Nabumetone
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220323
Marketing Category Name
ANDA
Application Number
ANDA078671
Manufacturer
American Health Packaging
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/60687-630-21