FDA — authorised 12 April 1988
- Application: NDA019508
- Marketing authorisation holder: SMITHKLINE BEECHAM
- Local brand name: AXID
- Indication: CAPSULE — ORAL
- Status: approved
FDA authorised Axid Capsule 150mg on 12 April 1988
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 12 April 1988; FDA authorised it on 25 May 2004; FDA has authorised it.
SMITHKLINE BEECHAM holds the US marketing authorisation.