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"0093-8072-56" National Drug Code (NDC)

Tiagabine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (0093-8072-56)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-8072-56
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0093-8072-56)
Product NDC0093-8072
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTiagabine Hydrochloride
Non-Proprietary NameTiagabine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180309
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA020646
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameTIAGABINE HYDROCHLORIDE
Strength12
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-8072-56





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