Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1CU Chemie Uetikon GmbH
02 1Changzhou Tianhua Pharmaceutical Co. Ltd.
03 1INNOVA PHARMACTIVE PRIVATE LIMITED
04 1LETCO MEDICAL, LLC
05 2Maithri Drugs Private Limited
06 1Medisca Inc.
07 2Professional Compounding Centers of America dba PCCA
08 1Yumen Qianhua Pharmaceutical Co., Ltd.
01 4METHIMAZOLE
02 1Methimazol
03 5Methimazole
01 1China
02 1France
03 3India
04 2U.S.A
05 2United Kingdom
06 1Blank
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 54382-112
Start Marketing Date : 1989-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66219-0253
Start Marketing Date : 2010-04-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70160-001
Start Marketing Date : 2022-06-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1515
Start Marketing Date : 2011-09-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0360
Start Marketing Date : 2009-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70600-032
Start Marketing Date : 2023-12-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70600-032
Start Marketing Date : 2021-12-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1943
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0326
Start Marketing Date : 2024-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 84317-102
Start Marketing Date : 2024-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Methimazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methimazole, including repackagers and relabelers. The FDA regulates Methimazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methimazole API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Methimazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methimazole supplier is an individual or a company that provides Methimazole active pharmaceutical ingredient (API) or Methimazole finished formulations upon request. The Methimazole suppliers may include Methimazole API manufacturers, exporters, distributors and traders.
click here to find a list of Methimazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Methimazole as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methimazole API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Methimazole as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Methimazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methimazole NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methimazole suppliers with NDC on PharmaCompass.
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