Drug company (FDA labeler)
Medi-Physics Inc. dba GE Healthcare.
NDC labeler code: 17156
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- TetrofosminMyoview · 2 products
- Indium IN-111 pentetate disodiumIndium Dtpa in 111 · 1 product
- Ioflupane I-123Datscan · 1 product
- Indium IN-111 oxyquinoline1 product
- Kit for the preparation of technetium tc 99M exametazime for leukocyte labelingDrax Exametazime, Ceretec · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| January 14, 2011 | NDA022454 | Ioflupane I-123 DATSCAN | Ge Hlthcare Inc |
| February 9, 1996 | NDA020372 | Tetrofosmin MYOVIEW, MYOVIEW 30ML | Medi-Physics |
| December 30, 1988 | NDA019829 | Kit for the preparation of technetium tc 99M exametazime for leukocyte labeling CERETEC | Ge Healthcare |
| December 24, 1985 | NDA019044 | Indium IN-111 oxyquinoline INDIUM IN 111 OXYQUINOLINE | Ge Healthcare |
| February 18, 1982 | NDA017707 | Indium IN-111 pentetate disodium MPI INDIUM DTPA IN 111 | Ge Healthcare |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026