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
31
PharmaCompass offers a list of Loperamide 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 Loperamide Hydrochloride manufacturer or Loperamide Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Loperamide Hydrochloride manufacturer or Loperamide Hydrochloride supplier.
PharmaCompass also assists you with knowing the Loperamide Hydrochloride API Price utilized in the formulation of products. Loperamide Hydrochloride API Price is not always fixed or binding as the Loperamide Hydrochloride Price is obtained through a variety of data sources. The Loperamide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IMODIUM MULTI-SYMPTOM RELIEF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IMODIUM MULTI-SYMPTOM RELIEF, including repackagers and relabelers. The FDA regulates IMODIUM MULTI-SYMPTOM RELIEF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IMODIUM MULTI-SYMPTOM RELIEF 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 IMODIUM MULTI-SYMPTOM RELIEF manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A IMODIUM MULTI-SYMPTOM RELIEF supplier is an individual or a company that provides IMODIUM MULTI-SYMPTOM RELIEF active pharmaceutical ingredient (API) or IMODIUM MULTI-SYMPTOM RELIEF finished formulations upon request. The IMODIUM MULTI-SYMPTOM RELIEF suppliers may include IMODIUM MULTI-SYMPTOM RELIEF API manufacturers, exporters, distributors and traders.
click here to find a list of IMODIUM MULTI-SYMPTOM RELIEF 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 IMODIUM MULTI-SYMPTOM RELIEF Drug Master File in Japan (IMODIUM MULTI-SYMPTOM RELIEF JDMF) empowers IMODIUM MULTI-SYMPTOM RELIEF 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 IMODIUM MULTI-SYMPTOM RELIEF JDMF during the approval evaluation for pharmaceutical products. At the time of IMODIUM MULTI-SYMPTOM RELIEF 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 IMODIUM MULTI-SYMPTOM RELIEF suppliers with JDMF on PharmaCompass.
We have 2 companies offering IMODIUM MULTI-SYMPTOM RELIEF
Get in contact with the supplier of your choice:
