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 2Daiwa Pharmaceutical Industries Co., Ltd.
03 1Dr. Reddy's Laboratories Ltd.
04 1Piramal Pharma Limited
05 1Yoshindo Co., Ltd.
01 1DILTIAZEM HYDROCHLORIDE
02 1Day stations diltiazem hydrochloride (production only)
03 1Diltiazem Hydrochloride
04 1Diltiazem hydrochloride "Teva / TIG"
05 1Diltiazem hydrochloride (production only)
06 1Japanese Pharmacopoeia drugs diltiazem hydrochloride (production only)
01 1Gabon
02 1India
03 1Israel
04 2Japan
05 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 : 2-3-5 Shimookui, 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 : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2017-03-07
Latest Date of Registration : 2017-03-07
Registration Number : 219MF10202
Registrant's Address : 7-1-27 AMEERPET HYDERABAD-500016-AP INDIA
Initial Date of Registration : 2007-06-13
Latest Date of Registration : 2007-06-13
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 Diacor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diacor, including repackagers and relabelers. The FDA regulates Diacor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diacor 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 Diacor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diacor supplier is an individual or a company that provides Diacor active pharmaceutical ingredient (API) or Diacor finished formulations upon request. The Diacor suppliers may include Diacor API manufacturers, exporters, distributors and traders.
click here to find a list of Diacor 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 Diacor Drug Master File in Japan (Diacor JDMF) empowers Diacor 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 Diacor JDMF during the approval evaluation for pharmaceutical products. At the time of Diacor 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 Diacor suppliers with JDMF on PharmaCompass.
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