"65841-773-77" National Drug Code (NDC)

NDC Code	65841-773-77
Package Description	10 BLISTER PACK in 1 CARTON (65841-773-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-773-30)
Product NDC	65841-773
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sirolimus
Non-Proprietary Name	Sirolimus
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20230216
Marketing Category Name	ANDA
Application Number	ANDA201676
Manufacturer	Zydus Lifesciences Limited
Substance Name	SIROLIMUS
Strength	2
Strength Unit	mg/1
Pharmacy Classes	Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]