Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
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01 1Metrochem API Pvt. Ltd.
02 1Daiwa Pharmaceutical Industries Co., Ltd.
03 1SperaNexus Inc.
04 1Yoshindo Co., Ltd.
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01 3Levocetirizine Hydrochloride
02 1Levocetirizine hydrochloride (manufacturing only)
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01 1India
02 3Japan
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Registration Number : 302MF10110
Registrant's Address : Flat No. 302, Bhanu Enclave, Sunder Nagar, Erragadda, Hyderabad - 500038, Telangana, ...
Initial Date of Registration : 2020-09-14
Latest Date of Registration : 2020-09-14
Registration Number : 230MF10147
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2018-11-05
Latest Date of Registration : 2018-11-05
Levocetirizine hydrochloride (for manufacturing purposes only)
Registration Number : 230MF10135
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2018-09-14
Latest Date of Registration : 2019-11-19
Registration Number : 230MF10149
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2018-11-07
Latest Date of Registration : 2018-11-07
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PharmaCompass offers a list of Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride manufacturer or Levocetirizine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levocetirizine Dihydrochloride manufacturer or Levocetirizine Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Levocetirizine Dihydrochloride API Price utilized in the formulation of products. Levocetirizine Dihydrochloride API Price is not always fixed or binding as the Levocetirizine Dihydrochloride Price is obtained through a variety of data sources. The Levocetirizine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A XYZAL ALLERGY 24HR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XYZAL ALLERGY 24HR, including repackagers and relabelers. The FDA regulates XYZAL ALLERGY 24HR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XYZAL ALLERGY 24HR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A XYZAL ALLERGY 24HR supplier is an individual or a company that provides XYZAL ALLERGY 24HR active pharmaceutical ingredient (API) or XYZAL ALLERGY 24HR finished formulations upon request. The XYZAL ALLERGY 24HR suppliers may include XYZAL ALLERGY 24HR API manufacturers, exporters, distributors and traders.
click here to find a list of XYZAL ALLERGY 24HR 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 XYZAL ALLERGY 24HR Drug Master File in Japan (XYZAL ALLERGY 24HR JDMF) empowers XYZAL ALLERGY 24HR 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 XYZAL ALLERGY 24HR JDMF during the approval evaluation for pharmaceutical products. At the time of XYZAL ALLERGY 24HR JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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