"68382-407-77" National Drug Code (NDC)

NDC Code	68382-407-77
Package Description	10 BLISTER PACK in 1 CARTON (68382-407-77) / 10 TABLET in 1 BLISTER PACK (68382-407-30)
Product NDC	68382-407
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Haloperidol
Non-Proprietary Name	Haloperidol
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20230201
Marketing Category Name	ANDA
Application Number	ANDA077580
Manufacturer	Zydus Pharmaceuticals USA Inc.
Substance Name	HALOPERIDOL
Strength	.5
Strength Unit	mg/1
Pharmacy Classes	Typical Antipsychotic [EPC]