"0781-1397-13" National Drug Code (NDC)

NDC Code	0781-1397-13
Package Description	10 BLISTER PACK in 1 CARTON (0781-1397-13) > 10 TABLET in 1 BLISTER PACK
Product NDC	0781-1397
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Haloperidol
Non-Proprietary Name	Haloperidol
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19880311
End Marketing Date	20201231
Marketing Category Name	ANDA
Application Number	ANDA071210
Manufacturer	Sandoz Inc
Substance Name	HALOPERIDOL
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Typical Antipsychotic [EPC]