Methyldopa - 42254-351-90 - (Methyldopa)

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Drug Information of Methyldopa

Product NDC: 42254-351
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: 42254-351
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070098
Marketing Category: ANDA
Start Marketing Date: 20090223

Package Information of Methyldopa

Package NDC: 42254-351-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (42254-351-90)

NDC Information of Methyldopa

NDC Code 42254-351-90
Proprietary Name Methyldopa
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (42254-351-90)
Product NDC 42254-351
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 Rebel Distributors Corp
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