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"68788-7220-3" National Drug Code (NDC)
Nabumetone 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7220-3)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7220-3
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7220-3)
Product NDC
68788-7220
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nabumetone
Non-Proprietary Name
Nabumetone
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180720
Marketing Category Name
ANDA
Application Number
ANDA091083
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
NABUMETONE
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7220-3