"67046-621-20" National Drug Code (NDC)

NDC Code	67046-621-20
Package Description	20 TABLET, FILM COATED in 1 BLISTER PACK (67046-621-20)
Product NDC	67046-621
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Quetiapine
Non-Proprietary Name	Quetiapine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20170926
Marketing Category Name	ANDA
Application Number	ANDA202152
Manufacturer	Contract Pharmacy Services-PA
Substance Name	QUETIAPINE FUMARATE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]