Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs Limited
02 1Alembic Pharmaceuticals Limited
03 1Amoli Organics (A Division of Umedica Laboratories Pvt Ltd.)
01 1Crude venlafaxine hydrochloride
02 1Venlafaxine Hydrochloride
03 1Blank
01 3India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Venlafaxine hydrochloride (NVF)
Registration Number : 305MF10133
Registrant's Address : 204 Udyog Kshetra 2nd Floor Mulund-Goregaon Link Road, Mulund (W), Mumbai 400080, Mah...
Initial Date of Registration : 2023-12-19
Latest Date of Registration : 2023-12-19
Registration Number : 304MF10131
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2022-09-21
Latest Date of Registration : 2022-09-21
Crude Venlafaxine Hydrochloride
Registration Number : 306MF10043
Registrant's Address : 407, Dalamal House, Jamnalal Bajaj Road, Nariman Point, Mumbai-400021. India.
Initial Date of Registration : 2024-03-13
Latest Date of Registration : 2024-03-13
A Effexor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Effexor, including repackagers and relabelers. The FDA regulates Effexor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Effexor 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 Effexor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Effexor supplier is an individual or a company that provides Effexor active pharmaceutical ingredient (API) or Effexor finished formulations upon request. The Effexor suppliers may include Effexor API manufacturers, exporters, distributors and traders.
click here to find a list of Effexor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Effexor Drug Master File in Japan (Effexor JDMF) empowers Effexor API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Effexor JDMF during the approval evaluation for pharmaceutical products. At the time of Effexor JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Effexor suppliers with JDMF on PharmaCompass.
We have 3 companies offering Effexor
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
