Methyldopa - 54569-0510-0 - (Methyldopa)

Alphabetical Index


Drug Information of Methyldopa

Product NDC: 54569-0510
Proprietary Name: Methyldopa
Non Proprietary Name: Methyldopa
Active Ingredient(s): 500    mg/1 & nbsp;   Methyldopa
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Methyldopa

Product NDC: 54569-0510
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070343
Marketing Category: ANDA
Start Marketing Date: 20090428

Package Information of Methyldopa

Package NDC: 54569-0510-0
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (54569-0510-0)

NDC Information of Methyldopa

NDC Code 54569-0510-0
Proprietary Name Methyldopa
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (54569-0510-0)
Product NDC 54569-0510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methyldopa
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090428
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
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