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"72205-084-30" National Drug Code (NDC)
Tiagabine Hydrochloride 30 TABLET in 1 BOTTLE (72205-084-30)
(Novadoz Pharmaceuticals LLC)
NDC Code
72205-084-30
Package Description
30 TABLET in 1 BOTTLE (72205-084-30)
Product NDC
72205-084
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tiagabine Hydrochloride
Non-Proprietary Name
Tiagabine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20211123
Marketing Category Name
ANDA
Application Number
ANDA214816
Manufacturer
Novadoz Pharmaceuticals LLC
Substance Name
TIAGABINE HYDROCHLORIDE
Strength
2
Strength Unit
mg/1
Pharmacy Classes
Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72205-084-30