"67046-620-21" National Drug Code (NDC)

NDC Code	67046-620-21
Package Description	21 TABLET, FILM COATED in 1 BLISTER PACK (67046-620-21)
Product NDC	67046-620
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	100
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]