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
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PharmaCompass offers a list of Venlafaxine 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 Venlafaxine Hydrochloride manufacturer or Venlafaxine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Venlafaxine Hydrochloride API Price utilized in the formulation of products. Venlafaxine Hydrochloride API Price is not always fixed or binding as the Venlafaxine Hydrochloride Price is obtained through a variety of data sources. The Venlafaxine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Effexor;Effexor XR;Efexor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Effexor;Effexor XR;Efexor, including repackagers and relabelers. The FDA regulates Effexor;Effexor XR;Efexor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Effexor;Effexor XR;Efexor 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 Effexor;Effexor XR;Efexor supplier is an individual or a company that provides Effexor;Effexor XR;Efexor active pharmaceutical ingredient (API) or Effexor;Effexor XR;Efexor finished formulations upon request. The Effexor;Effexor XR;Efexor suppliers may include Effexor;Effexor XR;Efexor API manufacturers, exporters, distributors and traders.
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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;Effexor XR;Efexor Drug Master File in Japan (Effexor;Effexor XR;Efexor JDMF) empowers Effexor;Effexor XR;Efexor 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;Effexor XR;Efexor JDMF during the approval evaluation for pharmaceutical products. At the time of Effexor;Effexor XR;Efexor JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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