"0591-2136-95" National Drug Code (NDC)

NDC Code	0591-2136-95
Package Description	25 VIAL in 1 CARTON (0591-2136-95) / 20 mL in 1 VIAL (0591-2136-80)
Product NDC	0591-2136
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Propofol
Non-Proprietary Name	Propofol
Dosage Form	INJECTION, EMULSION
Usage	INTRAVENOUS
Start Marketing Date	20160107
End Marketing Date	20230930
Marketing Category Name	ANDA
Application Number	ANDA205307
Manufacturer	Actavis Pharma, Inc.
Substance Name	PROPOFOL
Strength	10
Strength Unit	mg/mL
Pharmacy Classes	General Anesthesia [PE], General Anesthetic [EPC]