Holds 2 active US DMFs and one valid CEP for tizanidine, filing since 2001. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds 2 active US DMFs and one valid CEP for tizanidine, filing since 2019. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one valid CEP for tizanidine, filing since 2026. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 13 markets.
Holds one active US DMF for tizanidine, filing since 2020. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds one active US DMF for tizanidine, filing since 2008. Its 2025 FDA inspection closed as VAI.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Open the full list with a free accountThis page filters the worldwide Tizanidine manufacturer list to companies based in India. 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. Read the full method.
Tell us which markets you need to file in. These suppliers come back tiered for those markets, with the price corridor and an RFI sheet.
Start for free