01 1SNA Healthcare Pvt. Ltd.
01 1Sanil Pharma Co., Ltd.
01 1allantoin
01 1India
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2026-03-27
Registration Number : 20260327-211-J-2095
Manufacturer Name : SNA Healthcare Pvt. Ltd.
Manufacturer Address : Plot No. N-213/3, MIDC Industrial Area, Boisar, Tarapur Thane 401 506, Maharashtra St...
95
PharmaCompass offers a list of Glyoxyldiureide 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 Glyoxyldiureide manufacturer or Glyoxyldiureide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glyoxyldiureide manufacturer or Glyoxyldiureide supplier.
A Hemocane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hemocane, including repackagers and relabelers. The FDA regulates Hemocane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hemocane 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 Hemocane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hemocane supplier is an individual or a company that provides Hemocane active pharmaceutical ingredient (API) or Hemocane finished formulations upon request. The Hemocane suppliers may include Hemocane API manufacturers, exporters, distributors and traders.
click here to find a list of Hemocane 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 Hemocane Drug Master File in Korea (Hemocane KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Hemocane. The MFDS reviews the Hemocane KDMF as part of the drug registration process and uses the information provided in the Hemocane KDMF to evaluate the safety and efficacy of the drug.
After submitting a Hemocane 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 Hemocane API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Hemocane suppliers with KDMF on PharmaCompass.
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