01 1Olon S. p. A.
02 1Vasudha Pharma Chem Limited
01 1Loperamide Hydrochloride
02 1Loperamide hydrochloride
01 1India
02 1Italy
Registration Number : 217MF10757
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2020-10-01
Registration Number : 304MF10091
Registrant's Address : 78/A, Bengalrao Nagar, Hyderabad-500 038, Telangana State, India.
Initial Date of Registration : 2022-06-22
Latest Date of Registration : 2024-04-18
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PharmaCompass offers a list of Loperamide Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Loperamide Hydrochloride manufacturer or Loperamide Hydrochloride supplier for your needs.
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A Maalox Antidiarrheal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Maalox Antidiarrheal, including repackagers and relabelers. The FDA regulates Maalox Antidiarrheal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Maalox Antidiarrheal 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 Maalox Antidiarrheal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Maalox Antidiarrheal supplier is an individual or a company that provides Maalox Antidiarrheal active pharmaceutical ingredient (API) or Maalox Antidiarrheal finished formulations upon request. The Maalox Antidiarrheal suppliers may include Maalox Antidiarrheal API manufacturers, exporters, distributors and traders.
click here to find a list of Maalox Antidiarrheal suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Maalox Antidiarrheal Drug Master File in Japan (Maalox Antidiarrheal JDMF) empowers Maalox Antidiarrheal 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 Maalox Antidiarrheal JDMF during the approval evaluation for pharmaceutical products. At the time of Maalox Antidiarrheal 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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