"72611-860-04" National Drug Code (NDC)

NDC Code	72611-860-04
Package Description	4 VIAL, SINGLE-DOSE in 1 CARTON (72611-860-04) / 30 mL in 1 VIAL, SINGLE-DOSE (72611-860-01)
Product NDC	72611-860
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acetylcysteine
Non-Proprietary Name	Acetylcysteine
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20221017
End Marketing Date	20251201
Marketing Category Name	ANDA
Application Number	ANDA215620
Manufacturer	Almaject, Inc.
Substance Name	ACETYLCYSTEINE
Strength	200
Strength Unit	mg/mL
Pharmacy Classes	Antidote [EPC], Antidote for Acetaminophen Overdose [EPC], Decreased Respiratory Secretion Viscosity [PE], Increased Glutathione Concentration [PE], Mucolytic [EPC], Reduction Activity [MoA]