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01 1Teva API India Limited
02 1Zhejiang Chiral Medicine Chemicals Co., Ltd.
01 1METHYLDOPA
02 1Methyldopa
01 1China
02 1Israel
NDC Package Code : 15894-0038
Start Marketing Date : 2022-01-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67628-3001
Start Marketing Date : 2013-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Methyldopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyldopa, including repackagers and relabelers. The FDA regulates Methyldopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyldopa 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 Methyldopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methyldopa supplier is an individual or a company that provides Methyldopa active pharmaceutical ingredient (API) or Methyldopa finished formulations upon request. The Methyldopa suppliers may include Methyldopa API manufacturers, exporters, distributors and traders.
click here to find a list of Methyldopa 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 Methyldopa as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methyldopa 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 Methyldopa 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 Methyldopa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methyldopa NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methyldopa suppliers with NDC on PharmaCompass.
We have 2 companies offering Methyldopa
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