Veranova: A CDMO that manages complexity with confidence.
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01 1MACFARLAN SMITH LIMITED Edinburgh GB
02 1VERANOVA, L.P. West Deptford US
03 1SCI PHARMTECH, INC. Taoyuan City TW
04 1COHANCE LIFESCIENCES LIMITED Mumbai IN
05 2NORAMCO, LLC. Wilmington US
06 1BOEHRINGER INGELHEIM CHEMICALS INC. Ridgefield US
07 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
08 2HARMAN FINOCHEM LIMITED Mumbai IN
09 1IPCA Laboratories Limited Mumbai IN
10 1JANSSEN PHARMACEUTICA NV Beerse BE
11 1LABORATORIOS RUBIO, S.A. Castellbisbal ES
12 1SIEGFRIED EVIONNAZ SA Evionnaz CH
13 2SPECGX LLC Webster Groves US
14 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
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01 15Methylphenidate hydrochloride
02 1Methylphenidate hydrochloride, Process II
03 1Methylphenidate hydrochloride, Process II, Non-fine (Code 0570) and Fine (Code 1335)
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01 1Germany
02 6India
03 1Ireland
04 1Spain
05 1Switzerland
06 1Taiwan
07 5U.S.A
08 1United Kingdom
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01 15Valid
02 2Withdrawn by Holder
Certificate Number : CEP 2017-119 - Rev 01
Status : Valid
Issue Date : 2024-10-14
Type : Chemical
Substance Number : 2235
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Certificate Number : R1-CEP 2012-168 - Rev 01
Status : Valid
Issue Date : 2022-09-09
Type : Chemical
Substance Number : 2235
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2017-181 - Rev 02
Status : Valid
Issue Date : 2024-12-05
Type : Chemical
Substance Number : 2235
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Certificate Number : CEP 2018-030 - Rev 04
Status : Valid
Issue Date : 2024-09-26
Type : Chemical
Substance Number : 2235
Certificate Number : R1-CEP 2009-078 - Rev 00
Status : Valid
Issue Date : 2015-01-27
Type : Chemical
Substance Number : 2235
Certificate Number : CEP 2021-119 - Rev 02
Status : Valid
Issue Date : 2024-11-12
Type : Chemical
Substance Number : 2235
Certificate Number : R1-CEP 2009-094 - Rev 00
Status : Valid
Issue Date : 2015-08-03
Type : Chemical
Substance Number : 2235
Certificate Number : CEP 2009-219 - Rev 04
Status : Valid
Issue Date : 2024-12-23
Type : Chemical
Substance Number : 2235
Certificate Number : R1-CEP 2016-073 - Rev 00
Status : Valid
Issue Date : 2022-03-08
Type : Chemical
Substance Number : 2235
Certificate Number : R1-CEP 2011-378 - Rev 01
Status : Valid
Issue Date : 2018-10-19
Type : Chemical
Substance Number : 2235
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PharmaCompass offers a list of Methylphenidate 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 Methylphenidate Hydrochloride manufacturer or Methylphenidate Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methylphenidate Hydrochloride manufacturer or Methylphenidate Hydrochloride supplier.
PharmaCompass also assists you with knowing the Methylphenidate Hydrochloride API Price utilized in the formulation of products. Methylphenidate Hydrochloride API Price is not always fixed or binding as the Methylphenidate Hydrochloride Price is obtained through a variety of data sources. The Methylphenidate Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ritalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritalin, including repackagers and relabelers. The FDA regulates Ritalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritalin 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 Ritalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritalin supplier is an individual or a company that provides Ritalin active pharmaceutical ingredient (API) or Ritalin finished formulations upon request. The Ritalin suppliers may include Ritalin API manufacturers, exporters, distributors and traders.
click here to find a list of Ritalin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ritalin CEP of the European Pharmacopoeia monograph is often referred to as a Ritalin Certificate of Suitability (COS). The purpose of a Ritalin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ritalin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ritalin to their clients by showing that a Ritalin CEP has been issued for it. The manufacturer submits a Ritalin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ritalin CEP holder for the record. Additionally, the data presented in the Ritalin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ritalin DMF.
A Ritalin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ritalin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Ritalin suppliers with CEP (COS) on PharmaCompass.
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