"59746-002-04" National Drug Code (NDC)

NDC Code	59746-002-04
Package Description	25 TABLET in 1 BOTTLE (59746-002-04)
Product NDC	59746-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Methylprednisolone
Non-Proprietary Name	Methylprednisolone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19971031
End Marketing Date	20260501
Marketing Category Name	ANDA
Application Number	ANDA040189
Manufacturer	Jubilant Cadista Pharmaceuticals Inc.
Substance Name	METHYLPREDNISOLONE
Strength	8
Strength Unit	mg/1
Pharmacy Classes	Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]