"51079-200-20" National Drug Code (NDC)

NDC Code	51079-200-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-200-20) > 1 TABLET in 1 BLISTER PACK (51079-200-01)
Product NDC	51079-200
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Methyldopa
Non-Proprietary Name	Methyldopa
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19980901
End Marketing Date	20200131
Marketing Category Name	ANDA
Application Number	ANDA070076
Manufacturer	Mylan Institutional Inc.
Substance Name	METHYLDOPA
Strength	250
Strength Unit	mg/1
Pharmacy Classes	Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]