01 MACFARLAN SMITH LIMITED Edinburgh GB (1)
02 VERANOVA, L.P. West Deptford US (1)
03 SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN (1)
04 NORAMCO, LLC. Wilmington US (2)
05 BOEHRINGER INGELHEIM CHEMICALS INC. Ridgefield US (1)
06 CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN (1)
07 HARMAN FINOCHEM LIMITED Mumbai IN (2)
08 IPCA Laboratories Limited Mumbai IN (1)
09 JANSSEN PHARMACEUTICA NV Beerse BE (1)
10 LABORATORIOS RUBIO, S.A. Castellbisbal ES (1)
11 SCI PHARMTECH, INC. Taoyuan City TW (1)
12 SIEGFRIED EVIONNAZ SA Evionnaz CH (1)
13 SPECGX LLC Webster Groves US (2)
14 ZCL CHEMICALS LTD. Ankleshwar IN (1)
01 Methylphenidate hydrochloride (15)
02 Methylphenidate hydrochloride, Process II (1)
03 Methylphenidate hydrochloride, Process II, Non-fine (Code 0570) and Fine (Code 1335) (1)
01 Germany (1)
02 India (6)
03 Ireland (1)
04 Spain (1)
05 Switzerland (1)
06 Taiwan (1)
07 U.S.A (5)
08 United Kingdom (1)
01 Valid (15)
02 Withdrawn by Holder (2)
93
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 Daytrana manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Daytrana, including repackagers and relabelers. The FDA regulates Daytrana manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Daytrana 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 Daytrana manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Daytrana supplier is an individual or a company that provides Daytrana active pharmaceutical ingredient (API) or Daytrana finished formulations upon request. The Daytrana suppliers may include Daytrana API manufacturers, exporters, distributors and traders.
click here to find a list of Daytrana suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Daytrana CEP of the European Pharmacopoeia monograph is often referred to as a Daytrana Certificate of Suitability (COS). The purpose of a Daytrana CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Daytrana EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Daytrana to their clients by showing that a Daytrana CEP has been issued for it. The manufacturer submits a Daytrana CEP (COS) as part of the market authorization procedure, and it takes on the role of a Daytrana CEP holder for the record. Additionally, the data presented in the Daytrana CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Daytrana DMF.
A Daytrana CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Daytrana 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 Daytrana suppliers with CEP (COS) on PharmaCompass.
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