"0781-1396-13" National Drug Code (NDC)

NDC Code	0781-1396-13
Package Description	10 BLISTER PACK in 1 CARTON (0781-1396-13) > 10 TABLET in 1 BLISTER PACK
Product NDC	0781-1396
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Haloperidol
Non-Proprietary Name	Haloperidol
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19861117
End Marketing Date	20201231
Marketing Category Name	ANDA
Application Number	ANDA071209
Manufacturer	Sandoz Inc
Substance Name	HALOPERIDOL
Strength	5
Strength Unit	mg/1
Pharmacy Classes	Typical Antipsychotic [EPC]