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"52652-8001-1" National Drug Code (NDC)
Zonisade 1 BOTTLE in 1 CARTON (52652-8001-1) / 150 mL in 1 BOTTLE
(Azurity Phramaceuticals, Inc.)
NDC Code
52652-8001-1
Package Description
1 BOTTLE in 1 CARTON (52652-8001-1) / 150 mL in 1 BOTTLE
Product NDC
52652-8001
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Zonisade
Non-Proprietary Name
Zonisamide
Dosage Form
SUSPENSION
Usage
ORAL
Start Marketing Date
20220715
Marketing Category Name
NDA
Application Number
NDA214273
Manufacturer
Azurity Phramaceuticals, Inc.
Substance Name
ZONISAMIDE
Strength
100
Strength Unit
mg/5mL
Pharmacy Classes
Anti-epileptic Agent [EPC], Carbonic Anhydrase Inhibitors [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], P-Glycoprotein Inhibitors [MoA], Sulfonamides [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52652-8001-1