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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier.
A Cyclopentolate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclopentolate, including repackagers and relabelers. The FDA regulates Cyclopentolate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclopentolate 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 Cyclopentolate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cyclopentolate supplier is an individual or a company that provides Cyclopentolate active pharmaceutical ingredient (API) or Cyclopentolate finished formulations upon request. The Cyclopentolate suppliers may include Cyclopentolate API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclopentolate 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 Cyclopentolate Drug Master File in Korea (Cyclopentolate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cyclopentolate. The MFDS reviews the Cyclopentolate KDMF as part of the drug registration process and uses the information provided in the Cyclopentolate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cyclopentolate 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 Cyclopentolate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cyclopentolate suppliers with KDMF on PharmaCompass.
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