TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI Technology & API Services
02 2Ajinomoto Company
03 1Alfa Chemicals
04 1Daiichi Sankyo
05 1Divis Laboratories
06 2F. Hoffmann-La Roche
07 1GD Searle LLC
08 1Glochem Industries
09 1HOUSTON CYCLOTRON PARTNERS LP
10 1Hetero Drugs
11 1Key Pharmaceuticals
12 1Maithri Drugs
13 1PVP Sociedade Anonima
14 1Plantex Ltd.
15 1Shandong Xinhua Pharmaceutical
16 1Zhejiang Huahai Pharmaceutical
17 1Zhejiang Wild Wind Pharmaceutical Co
18 1elm-plastic GmbH
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2024-04-12
Pay. Date : 2017-09-08
DMF Number : 32057
Submission : 2020-06-29
Status :
Type : II
A Levodopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levodopa, including repackagers and relabelers. The FDA regulates Levodopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levodopa 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 Levodopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levodopa supplier is an individual or a company that provides Levodopa active pharmaceutical ingredient (API) or Levodopa finished formulations upon request. The Levodopa suppliers may include Levodopa API manufacturers, exporters, distributors and traders.
click here to find a list of Levodopa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levodopa DMF (Drug Master File) is a document detailing the whole manufacturing process of Levodopa active pharmaceutical ingredient (API) in detail. Different forms of Levodopa DMFs exist exist since differing nations have different regulations, such as Levodopa USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Levodopa DMF submitted to regulatory agencies in the US is known as a USDMF. Levodopa USDMF includes data on Levodopa's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Levodopa USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Levodopa suppliers with USDMF on PharmaCompass.
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