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, Price,and more, enabling you to easily find the right Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Cyclopentolate Hydrochloride API Price utilized in the formulation of products. Cyclopentolate Hydrochloride API Price is not always fixed or binding as the Cyclopentolate Hydrochloride Price is obtained through a variety of data sources. The Cyclopentolate Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zyklolat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zyklolat, including repackagers and relabelers. The FDA regulates Zyklolat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zyklolat 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 Zyklolat supplier is an individual or a company that provides Zyklolat active pharmaceutical ingredient (API) or Zyklolat finished formulations upon request. The Zyklolat suppliers may include Zyklolat API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Zyklolat Drug Master File in Korea (Zyklolat KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zyklolat. The MFDS reviews the Zyklolat KDMF as part of the drug registration process and uses the information provided in the Zyklolat KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zyklolat 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 Zyklolat API can apply through the Korea Drug Master File (KDMF).
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