NDC 68151-2791

Methyldopa

Methyldopa

Methyldopa is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Methyldopa.

Product ID68151-2791_29a33fb6-f519-4c20-8dc4-c5286f79fbd2
NDC68151-2791
Product TypeHuman Prescription Drug
Proprietary NameMethyldopa
Generic NameMethyldopa
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2012-07-24
Marketing CategoryANDA / ANDA
Application NumberANDA070084
Labeler NameCarilion Materials Management
Substance NameMETHYLDOPA
Active Ingredient Strength250 mg/1
Pharm ClassesAdrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68151-2791-5

1 TABLET, FILM COATED in 1 BOTTLE (68151-2791-5)
Marketing Start Date2012-07-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68151-2791-5 [68151279105]

Methyldopa TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA070084
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-07-24
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
METHYLDOPA250 mg/1

OpenFDA Data

SPL SET ID:e503c0bf-c326-48fb-8967-0f476eaa8961
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197956
  • Pharmacological Class

    • Adrenergic alpha2-Agonists [MoA]
    • Central alpha-2 Adrenergic Agonist [EPC]

    NDC Crossover Matching brand name "Methyldopa" or generic name "Methyldopa"

    NDCBrand NameGeneric Name
    0378-0421Methyldopamethyldopa
    0378-0611Methyldopamethyldopa
    16729-030MethyldopaMethyldopa
    16729-031MethyldopaMethyldopa
    21695-879MethyldopaMethyldopa
    21695-880MethyldopaMethyldopa
    42254-351MethyldopaMethyldopa
    51079-200Methyldopamethyldopa
    51079-201Methyldopamethyldopa
    62135-321MethyldopaMethyldopa
    62135-322MethyldopaMethyldopa
    68151-2791MethyldopaMethyldopa

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