NDC 68788-8926

Methimazole

Methimazole

Methimazole is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Methimazole.

Product ID68788-8926_3e07c8c9-5474-45dd-921c-b95bed8e7024
NDC68788-8926
Product TypeHuman Prescription Drug
Proprietary NameMethimazole
Generic NameMethimazole
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-10-06
Marketing CategoryANDA / ANDA
Application NumberANDA040734
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameMETHIMAZOLE
Active Ingredient Strength5 mg/1
Pharm ClassesThyroid Hormone Synthesis Inhibitor [EPC],Thyroid Hormone Synthesis Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-8926-9

90 TABLET in 1 BOTTLE (68788-8926-9)
Marketing Start Date2015-10-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-8926-9 [68788892609]

Methimazole TABLET
Marketing CategoryANDA
Application NumberANDA040734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-06
Marketing End Date2019-10-28

NDC 68788-8926-1 [68788892601]

Methimazole TABLET
Marketing CategoryANDA
Application NumberANDA040734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-06
Marketing End Date2019-10-28

NDC 68788-8926-3 [68788892603]

Methimazole TABLET
Marketing CategoryANDA
Application NumberANDA040734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-06
Marketing End Date2019-10-28

NDC 68788-8926-2 [68788892602]

Methimazole TABLET
Marketing CategoryANDA
Application NumberANDA040734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-06
Marketing End Date2019-10-28

NDC 68788-8926-6 [68788892606]

Methimazole TABLET
Marketing CategoryANDA
Application NumberANDA040734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-10-06
Marketing End Date2019-10-28

Drug Details

Active Ingredients

IngredientStrength
METHIMAZOLE5 mg/1

OpenFDA Data

SPL SET ID:aac32d35-4b37-4988-af70-ebc5ad069b4f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197942
  • Pharmacological Class

    • Thyroid Hormone Synthesis Inhibitor [EPC]
    • Thyroid Hormone Synthesis Inhibitors [MoA]

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

    NDCBrand NameGeneric Name
    0185-0205MethimazoleMethimazole
    0185-0210MethimazoleMethimazole
    0615-6500MethimazoleMethimazole
    0615-7613MethimazoleMethimazole
    23155-070MethimazoleMethimazole
    23155-071MethimazoleMethimazole
    42254-008Methimazolemethimazole
    42254-009Methimazolemethimazole
    49884-640Methimazolemethimazole
    49884-641Methimazolemethimazole
    50090-2366Methimazolemethimazole
    50090-3334Methimazolemethimazole
    50436-7066MethimazoleMethimazole
    51293-820MethimazoleMethimazole
    51293-821MethimazoleMethimazole
    53808-0850Methimazolemethimazole
    53808-0949MethimazoleMethimazole
    53808-1044METHIMAZOLEMETHIMAZOLE
    60429-380MethimazoleMethimazole
    60429-381MethimazoleMethimazole
    60687-357Methimazolemethimazole
    60687-370Methimazolemethimazole
    68071-3027MethimazoleMethimazole
    68084-275MethimazoleMethimazole
    68084-276MethimazoleMethimazole
    68788-0681METHIMAZOLEMETHIMAZOLE
    68788-8926MethimazoleMethimazole
    70518-1475MethimazoleMethimazole
    70518-1506MethimazoleMethimazole
    71335-0883MethimazoleMethimazole
    63629-6408MethimazoleMethimazole
    64980-260MethimazoleMethimazole
    64980-261MethimazoleMethimazole
    66336-623MethimazoleMethimazole

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.