Methyldopa - 0093-2931-01 - (Methyldopa)

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Drug Information of Methyldopa

Product NDC: 0093-2931
Proprietary Name: Methyldopa
Non Proprietary Name: Methyldopa
Active Ingredient(s): 250    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: 0093-2931
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070098
Marketing Category: ANDA
Start Marketing Date: 20090223

Package Information of Methyldopa

Package NDC: 0093-2931-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-2931-01)

NDC Information of Methyldopa

NDC Code 0093-2931-01
Proprietary Name Methyldopa
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-2931-01)
Product NDC 0093-2931
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methyldopa
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090223
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name METHYLDOPA
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Methyldopa


General Information