Veranova: A CDMO that manages complexity with confidence.
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
01 15Methylphenidate hydrochloride
02 1Methylphenidate hydrochloride, Process II
03 1Methylphenidate hydrochloride, Process II, Non-fine (Code 0570) and Fine (Code 1335)
01 1Germany
02 6India
03 1Ireland
04 1Spain
05 1Switzerland
06 1Taiwan
07 5U.S.A
08 1United Kingdom
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 2010-031 - Rev 02
Status : Valid
Issue Date : 2022-04-08
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 : CEP 2009-359 - Rev 02
Status : Valid
Issue Date : 2024-03-05
Type : Chemical
Substance Number : 2235
A Methylphenidate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylphenidate Hydrochloride, including repackagers and relabelers. The FDA regulates Methylphenidate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylphenidate Hydrochloride 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 Methylphenidate Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylphenidate Hydrochloride supplier is an individual or a company that provides Methylphenidate Hydrochloride active pharmaceutical ingredient (API) or Methylphenidate Hydrochloride finished formulations upon request. The Methylphenidate Hydrochloride suppliers may include Methylphenidate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Methylphenidate Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methylphenidate Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Methylphenidate Hydrochloride Certificate of Suitability (COS). The purpose of a Methylphenidate Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Methylphenidate Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Methylphenidate Hydrochloride to their clients by showing that a Methylphenidate Hydrochloride CEP has been issued for it. The manufacturer submits a Methylphenidate Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Methylphenidate Hydrochloride CEP holder for the record. Additionally, the data presented in the Methylphenidate Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Methylphenidate Hydrochloride DMF.
A Methylphenidate Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Methylphenidate Hydrochloride 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 Methylphenidate Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 13 companies offering Methylphenidate Hydrochloride
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