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"72205-087-30" National Drug Code (NDC)
Tiagabine Hydrochloride 30 TABLET in 1 BOTTLE (72205-087-30)
(Novadoz Pharmaceuticals LLC)
NDC Code
72205-087-30
Package Description
30 TABLET in 1 BOTTLE (72205-087-30)
Product NDC
72205-087
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
16
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/72205-087-30