"72572-151-10" National Drug Code (NDC)

NDC Code	72572-151-10
Package Description	1 VIAL, SINGLE-DOSE in 1 CARTON (72572-151-10) / 1 mL in 1 VIAL, SINGLE-DOSE (72572-151-01)
Product NDC	72572-151
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ephedrine Sulfate
Non-Proprietary Name	Ephedrine Sulfate
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20210823
Marketing Category Name	ANDA
Application Number	ANDA212932
Manufacturer	Civica, Inc.
Substance Name	EPHEDRINE SULFATE
Strength	50
Strength Unit	mg/mL
Pharmacy Classes	Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]