🇺🇸 Lignospan Forte in United States

FDA authorised Lignospan Forte on 14 January 1986

Marketing authorisations

FDA — authorised 14 January 1986

  • Application: ANDA088389
  • Marketing authorisation holder: DEPROCO
  • Local brand name: LIGNOSPAN FORTE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA

  • Status: approved

Lignospan Forte in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Neuroscience approved in United States

Frequently asked questions

Is Lignospan Forte approved in United States?

Yes. FDA authorised it on 14 January 1986; FDA has authorised it.

Who is the marketing authorisation holder for Lignospan Forte in United States?

DEPROCO holds the US marketing authorisation.