FDA — authorised 14 January 1986
- Application: ANDA088389
- Marketing authorisation holder: DEPROCO
- Local brand name: LIGNOSPAN FORTE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Lignospan Forte on 14 January 1986
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 14 January 1986; FDA has authorised it.
DEPROCO holds the US marketing authorisation.