Holds one active US DMF and one valid CEP for mepivacaine, filing since 2006. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF and one valid CEP for mepivacaine, filing since 1979. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for mepivacaine, filing since 2020. Its 2022 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for mepivacaine, filing since 1983.
Registered with SFDA (Saudi Arabia) for mepivacaine. Its 2023 FDA inspection closed as VAI.
The names are listed below. Ask Fred about the filings, inspection history and GMP certificates on record for each manufacturer.
Chat with Fred, your AI analystContract manufacturers make to order rather than holding their own filing for this molecule.
The order is set by active filings weighted by regulator, inspection outcomes and their recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags. Every factor appears on the card it produced. Read the full method.
Ask Fred which manufacturers are on record for mepivacaine and what filings they hold.
Chat with Fred, your AI analyst