"55292-701-55" National Drug Code (NDC)

NDC Code	55292-701-55
Package Description	1 VIAL in 1 CARTON (55292-701-55) > 43 mL in 1 VIAL (55292-701-54)
Product NDC	55292-701
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Panhematin
Non-Proprietary Name	Hemin
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	19830720
End Marketing Date	20200124
Marketing Category Name	BLA
Application Number	BLA101246
Manufacturer	RECORDATI RARE DISEASES, INC.
Substance Name	HEMIN
Strength	7
Strength Unit	mg/mL