"68382-239-80" National Drug Code (NDC)

NDC Code	68382-239-80
Package Description	8 BLISTER PACK in 1 CARTON (68382-239-80) > 10 CAPSULE in 1 BLISTER PACK (68382-239-30)
Product NDC	68382-239
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ziprasidone
Non-Proprietary Name	Ziprasidone
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20171228
Marketing Category Name	ANDA
Application Number	ANDA208988
Manufacturer	Zydus Pharmaceuticals (USA) Inc.
Substance Name	ZIPRASIDONE HYDROCHLORIDE
Strength	60
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]