FDA — authorised 1 August 1977
- Application: NDA018012
- Marketing authorisation holder: SPECGX LLC
- Local brand name: PAMELOR
- Indication: SOLUTION — ORAL
- Status: approved
FDA authorised Switch to nortriptyline on 1 August 1977
Yes. FDA authorised it on 1 August 1977; FDA authorised it on 1 August 1977.
SPECGX LLC holds the US marketing authorisation.