Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1M/s Cohance Lifesciences Limited
02 1M/s Centaur Pharmaceuticals Pvt Ltd
03 1M/s Harman Finochem limited
04 1M/s IPCA Laboratories Ltd
05 1M/s Sun Pharmaceuticals Industries ltd
01 1Methyl Phenidate Hydrochloride BP/EP/USP
02 1Methyl Phenidate Hydrochloride EP/IH
03 1Methylphenidate Hydrochloride BP/Ph.Eur./USP
04 1Methylphenidate Hydrochloride EP/USP
05 1Methylphenidate Hydrochloride USP/Ph.Eur.
01 1WC-0045nA2
02 1WC-0091n
03 1WC-0107
04 1WC-0168
05 1WC-0195
01 5India
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Methyl Phenidate Hydrochloride EP/IH
Date of Issue : 2022-08-25
Valid Till : 2025-02-07
Written Confirmation Number : WC-0195
Address of the Firm : Plot No. 3102/B, GIDC Estate Ankleshwar, Bharuch-393002, Gujarat, India
Methyl Phenidate Hydrochloride BP/EP/USP
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm : Plot No. 75/76, 76/1 & 74, Chikhloli MIDC, Ambernath (West), Thane- 421501, Maha...
Methylphenidate Hydrochloride EP/USP
Date of Issue : 2022-08-06
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm : Plot No. E-7, E-8, E-9, MIDC Industrial Area, Chikalthana, Aurangabad-431006
Methylphenidate Hydrochloride BP/Ph.Eur./USP
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091n
Address of the Firm : P.O. Sejavta, Dist. Ratlam, Madhya Pradesh, India.
Methylphenidate Hydrochloride USP/Ph.Eur.
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm : Plot No. 24/2, & 25, Phase -IV, GIDC Industrial Zone, At & Post - Panoli, Dist.-...
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A Quillivant xr (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quillivant xr (TN), including repackagers and relabelers. The FDA regulates Quillivant xr (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quillivant xr (TN) 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 Quillivant xr (TN) supplier is an individual or a company that provides Quillivant xr (TN) active pharmaceutical ingredient (API) or Quillivant xr (TN) finished formulations upon request. The Quillivant xr (TN) suppliers may include Quillivant xr (TN) API manufacturers, exporters, distributors and traders.
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A Quillivant xr (TN) written confirmation (Quillivant xr (TN) WC) is an official document issued by a regulatory agency to a Quillivant xr (TN) manufacturer, verifying that the manufacturing facility of a Quillivant xr (TN) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Quillivant xr (TN) APIs or Quillivant xr (TN) finished pharmaceutical products to another nation, regulatory agencies frequently require a Quillivant xr (TN) WC (written confirmation) as part of the regulatory process.
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