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 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 : 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
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 Diltia XT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diltia XT, including repackagers and relabelers. The FDA regulates Diltia XT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diltia XT 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 Diltia XT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diltia XT supplier is an individual or a company that provides Diltia XT active pharmaceutical ingredient (API) or Diltia XT finished formulations upon request. The Diltia XT suppliers may include Diltia XT API manufacturers, exporters, distributors and traders.
click here to find a list of Diltia XT 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 Diltia XT Drug Master File in Japan (Diltia XT JDMF) empowers Diltia XT 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 Diltia XT JDMF during the approval evaluation for pharmaceutical products. At the time of Diltia XT 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 Diltia XT suppliers with JDMF on PharmaCompass.
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