FDA — authorised 26 June 1986
- Application: NDA018962
- Marketing authorisation holder: HOSPIRA
- Local brand name: MANGANESE CHLORIDE IN PLASTIC CONTAINER
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Manganese Chloride In Plastic Container on 26 June 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 26 June 1986; FDA authorised it on 19 December 1997; FDA authorised it on 7 July 2025.
HOSPIRA holds the US marketing authorisation.