Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
01 1Tagoor Laboratories Private Limited
02 1Cadila Healthcare Limited
03 1Cadila Limited
04 4Cadila Pharmaceuticals Limited
05 5Cadila Pharmaceuticals Limited.
06 1Cadila Pharmaceuticals Ltd.
07 1MSD International GmbH (Singapore Branch)
08 2Mylan Laboratories Limited
09 1Schering-Plough (Avondale) Co
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2025-04-16
Registration Number : 20250416-6-C-429-08
Manufacturer Name : Tagoor Laboratories Private ...
Manufacturer Address : Unit-III,Plot No.12, JNPharma City, Parawada (mdl), Anakapalli Dist.-531021, Andhra P...
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PharmaCompass offers a list of Loratadine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Loratadine manufacturer or Loratadine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Loratadine manufacturer or Loratadine supplier.
PharmaCompass also assists you with knowing the Loratadine API Price utilized in the formulation of products. Loratadine API Price is not always fixed or binding as the Loratadine Price is obtained through a variety of data sources. The Loratadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sinhistan Dy manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sinhistan Dy, including repackagers and relabelers. The FDA regulates Sinhistan Dy manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sinhistan Dy API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sinhistan Dy supplier is an individual or a company that provides Sinhistan Dy active pharmaceutical ingredient (API) or Sinhistan Dy finished formulations upon request. The Sinhistan Dy suppliers may include Sinhistan Dy API manufacturers, exporters, distributors and traders.
click here to find a list of Sinhistan Dy suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Sinhistan Dy Drug Master File in Korea (Sinhistan Dy KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sinhistan Dy. The MFDS reviews the Sinhistan Dy KDMF as part of the drug registration process and uses the information provided in the Sinhistan Dy KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sinhistan Dy KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Sinhistan Dy API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sinhistan Dy suppliers with KDMF on PharmaCompass.
We have 4 companies offering Sinhistan Dy
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