Methyldopa - 51079-201-20 - (methyldopa)

Alphabetical Index


Drug Information of Methyldopa

Product NDC: 51079-201
Proprietary Name: Methyldopa
Non Proprietary Name: methyldopa
Active Ingredient(s): 500    mg/1 & nbsp;   methyldopa
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methyldopa

Product NDC: 51079-201
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070076
Marketing Category: ANDA
Start Marketing Date: 20121212

Package Information of Methyldopa

Package NDC: 51079-201-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-201-20) > 1 TABLET in 1 BLISTER PACK (51079-201-01)

NDC Information of Methyldopa

NDC Code 51079-201-20
Proprietary Name Methyldopa
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-201-20) > 1 TABLET in 1 BLISTER PACK (51079-201-01)
Product NDC 51079-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methyldopa
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121212
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name METHYLDOPA
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Methyldopa


General Information