Sumatriptan
Overview
Sumatriptan is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL128).
API suppliers (14)
Suppliers of Sumatriptan evidenced by a US FDA Type II Drug Master File or an EU Certificate of Suitability (CEP). Sources: FDA DMF list, EDQM certification database.
Country recorded for 12 of 14 suppliers.
9 of 14 hold a GMP certificate on record in the EU or UK registers
- SMS Pharmaceuticals limitedIndia2 active DMF GMP on record
- APITORIA PHARMA PRIVATE LTDIndia2 active DMF GMP on record
- MSN PHARMACHEM PRIVATE LTDIndia2 active DMF
- Sun Pharmaceutical Industries LimitedIndia1 active DMF GMP on record
- MATRIX PHARMACORP PRIVATE LTDIndia1 active DMF
- Divis LaboratoriesIndia1 active DMF GMP on record
- Natco PharmaIndia1 active DMF GMP on record
- MOEHS IBERICA SLSpain1 active DMF GMP on record
- CHROMO LABORATORIES INDIA PRIVATE LTDIndia1 active DMF
- DR REDDYS LABORATORIES LTD1 active DMF GMP on record
- QUIMICA SINTETICA SASpain GMP on record
- APOTEX PHARMACHEM INC
- Hovione FarmaCiencia SAPortugal GMP on record
- Cipla USA, Inc.USA
Patent & exclusivity (US)
Per the FDA Orange Book (52 approved US products), the latest listed US patent on Sumatriptan expires 29 Jan 2036. Generic API sourcing typically opens up once these lapse.
Chemical identity
- IUPAC name
- 1-[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]-N-methylmethanesulfonamide
- Canonical SMILES
- CNS(=O)(=O)CC1=CC2=C(C=C1)NC=C2CCN(C)C
- InChIKey
- KQKPFRSPSRPDEB-UHFFFAOYSA-N
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