01 1Laurus Labs Limited (Unit-4)
01 1Masung LS Co., Ltd.
01 1Cyclopentolate hydrochloride
01 1India
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2025-12-11
Registration Number : 20251211-211-J-2087
Manufacturer Name : Laurus Labs Limited (Unit-4)
Manufacturer Address : Plot No. 25, 25A to 25K, APSEZ, De-Notified Area, Lalamkoduru Village, Rambilli Manda...
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PharmaCompass offers a list of Cyclopentolate Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier for your needs.
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A Cicloplegicedol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cicloplegicedol, including repackagers and relabelers. The FDA regulates Cicloplegicedol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cicloplegicedol 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 Cicloplegicedol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cicloplegicedol supplier is an individual or a company that provides Cicloplegicedol active pharmaceutical ingredient (API) or Cicloplegicedol finished formulations upon request. The Cicloplegicedol suppliers may include Cicloplegicedol API manufacturers, exporters, distributors and traders.
click here to find a list of Cicloplegicedol suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Cicloplegicedol Drug Master File in Korea (Cicloplegicedol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cicloplegicedol. The MFDS reviews the Cicloplegicedol KDMF as part of the drug registration process and uses the information provided in the Cicloplegicedol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cicloplegicedol 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 Cicloplegicedol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cicloplegicedol suppliers with KDMF on PharmaCompass.
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