Cardiogen 82 first approval in a eu country?

What was Cardiogen 82’s first approval in an EU country?

The provided information doesn’t include enough details to identify Cardiogen 82’s first marketing authorization date or which EU country granted the initial approval.

What I need to pinpoint the “first approval” country and date

To answer accurately, I need at least one of the following:
- The full product name as used in the EU (and whether “Cardiogen 82” is the brand or a generic/atom/radiopharmaceutical reference)
- The active substance (and any strength/formulation details)
- The MAH/marketing authorization holder name
- An authorization/registration number, or a link to the product’s EU listing

With that, I can determine which EU regulator approved it first (and the date), then cite the source.

Where approval records are usually found for EU radiopharmaceuticals

If you can share the product identifiers above, I can check the relevant public EU/regulatory listings to find:
- The earliest country-level marketing authorization (first EU approval)
- The MAH at the time of first approval
- Whether the product later moved into a centralized/renewed authorization route

Quick next step

Reply with the active ingredient and dosage form (or paste the EU product label text / authorization holder). Once I have that, I’ll tell you the first EU country approval and the approval date, with a source link.