FDA — authorised 7 March 1997
- Status: approved
🇺🇸 Skelid in United States
FDA authorised Skelid on 7 March 1997
Marketing authorisations
FDA — authorised 7 March 1997
- Application: NDA020707
- Marketing authorisation holder: SANOFI AVENTIS US
- Local brand name: SKELID
- Indication: TABLET — ORAL
- Status: approved
Skelid in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Other Bone approved in United States
Frequently asked questions
Is Skelid approved in United States?
Yes. FDA authorised it on 7 March 1997; FDA authorised it on 7 March 1997.
Who is the marketing authorisation holder for Skelid in United States?
Marketing authorisation holder not available in our data.