TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Limited
02 2Daito Co., Ltd.
03 1Piramal Pharma Limited
04 1Yoshindo Co., Ltd.
01 1Day stations diltiazem hydrochloride (production only)
02 1Diltiazem Hydrochloride
03 1Diltiazem hydrochloride "Teva / TIG"
04 1Diltiazem hydrochloride (production only)
05 1Japanese Pharmacopoeia drugs diltiazem hydrochloride (production only)
01 1India
02 1Israel
03 2Japan
04 1U.S.A
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Diltiazem hydrochloride "Teva/TIG"
Registration Number : 225MF10001
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2013-01-15
Latest Date of Registration : 2013-01-15
Japanese Pharmacopoeia Diltiazem Hydrochloride (for manufacturing only)
Registration Number : 219MF10031
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-02-05
Latest Date of Registration : 2013-02-20
Registration Number : 221MF10252
Registrant's Address : Digwal Village (Sy.Nos.7-70, 70/1 and 70/2), Kohir Mandal, Sangareddy District-502 32...
Initial Date of Registration : 2009-11-24
Latest Date of Registration : 2014-07-01
Diltiazem hydrochloride (for manufacturing only)
Registration Number : 229MF10062
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2017-03-07
Latest Date of Registration : 2017-03-07
JP Diltiazem Hydrochloride (for manufacturing only)
Registration Number : 218MF10126
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2007-05-15
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PharmaCompass offers a list of Diltiazem 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 Diltiazem Hydrochloride manufacturer or Diltiazem Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diltiazem Hydrochloride manufacturer or Diltiazem Hydrochloride supplier.
PharmaCompass also assists you with knowing the Diltiazem Hydrochloride API Price utilized in the formulation of products. Diltiazem Hydrochloride API Price is not always fixed or binding as the Diltiazem Hydrochloride Price is obtained through a variety of data sources. The Diltiazem Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Myonil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Myonil, including repackagers and relabelers. The FDA regulates Myonil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Myonil 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 Myonil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Myonil supplier is an individual or a company that provides Myonil active pharmaceutical ingredient (API) or Myonil finished formulations upon request. The Myonil suppliers may include Myonil API manufacturers, exporters, distributors and traders.
click here to find a list of Myonil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Myonil Drug Master File in Japan (Myonil JDMF) empowers Myonil 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 Myonil JDMF during the approval evaluation for pharmaceutical products. At the time of Myonil JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Myonil suppliers with JDMF on PharmaCompass.
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