With Virupaksha, you get a quality product with on-time delivery.
01 1Virupaksha Organics Ltd, Unit-I
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15 1UK Chemical Farm Co., Ltd.
16 1Zhejiang Huahai Pharmaceutical Co., Ltd.
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With Virupaksha, you get a quality product with on-time delivery.
Registrant Name : Toru Corporation
Registration Date : 2023-08-23
Registration Number : 20230823-209-J-1539
Manufacturer Name : Virupaksha Organics Ltd, Uni...
Manufacturer Address : 502 319, Sy.No.10, Gaddapotharam Village, Jinnaram Mandal, Medak District, Andhra Pra...
Neuland Laboratories- A dedicated 100% API provider.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2023-09-19
Registration Number : 20230919-209-J-1546
Manufacturer Name : Neuland Laboratories Limited
Manufacturer Address : Unit-I, Sy. No. 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy Temple Ro...
A Escitalopram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Escitalopram, including repackagers and relabelers. The FDA regulates Escitalopram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Escitalopram 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 Escitalopram manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Escitalopram supplier is an individual or a company that provides Escitalopram active pharmaceutical ingredient (API) or Escitalopram finished formulations upon request. The Escitalopram suppliers may include Escitalopram API manufacturers, exporters, distributors and traders.
click here to find a list of Escitalopram 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 Escitalopram Drug Master File in Korea (Escitalopram KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Escitalopram. The MFDS reviews the Escitalopram KDMF as part of the drug registration process and uses the information provided in the Escitalopram KDMF to evaluate the safety and efficacy of the drug.
After submitting a Escitalopram 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 Escitalopram API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Escitalopram suppliers with KDMF on PharmaCompass.
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