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PharmaCompass offers a list of Levonorgestrel 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 Levonorgestrel manufacturer or Levonorgestrel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levonorgestrel manufacturer or Levonorgestrel supplier.
PharmaCompass also assists you with knowing the Levonorgestrel API Price utilized in the formulation of products. Levonorgestrel API Price is not always fixed or binding as the Levonorgestrel Price is obtained through a variety of data sources. The Levonorgestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ALTAVERA-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALTAVERA-1, including repackagers and relabelers. The FDA regulates ALTAVERA-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALTAVERA-1 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 ALTAVERA-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALTAVERA-1 supplier is an individual or a company that provides ALTAVERA-1 active pharmaceutical ingredient (API) or ALTAVERA-1 finished formulations upon request. The ALTAVERA-1 suppliers may include ALTAVERA-1 API manufacturers, exporters, distributors and traders.
click here to find a list of ALTAVERA-1 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 ALTAVERA-1 Drug Master File in Japan (ALTAVERA-1 JDMF) empowers ALTAVERA-1 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 ALTAVERA-1 JDMF during the approval evaluation for pharmaceutical products. At the time of ALTAVERA-1 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 ALTAVERA-1 suppliers with JDMF on PharmaCompass.
We have 4 companies offering ALTAVERA-1
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