FDA — authorised 19 April 1983
- Application: NDA018553
- Marketing authorisation holder: ANI PHARMS
- Local brand name: INDERAL LA
- Indication: CAPSULE, EXTENDED RELEASE — ORAL
- Status: approved
FDA authorised Inderal-LA on 19 April 1983
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 19 April 1983; FDA has authorised it.
ANI PHARMS holds the US marketing authorisation.