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"62756-200-18" National Drug Code (NDC)

Tiagabine Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (62756-200-18)
(Sun Pharmaceutical Industries, Inc.)

NDC Code62756-200-18
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (62756-200-18)
Product NDC62756-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTiagabine Hydrochloride
Non-Proprietary NameTiagabine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20111104
Marketing Category NameANDA
Application NumberANDA077555
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameTIAGABINE HYDROCHLORIDE
Strength2
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/62756-200-18





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