Quick answers
- What is Draximage Dtpa?
- Draximage Dtpa is a brand name of Kit for the preparation of technetium tc 99M pentetate, a prescription medicine. The FDA NDC Directory lists 1 Draximage Dtpa product in 1 strength and form.
- Who makes Draximage Dtpa?
- Jubilant holds the FDA application for Draximage Dtpa (NDA018511, approved December 29, 1989).
- Is there a generic or store brand of Draximage Dtpa?
- Other products of Kit for the preparation of technetium tc 99M pentetate are listed with the FDA, but none in exactly the same strength and form as a Draximage Dtpa product.
- Has Draximage Dtpa been recalled?
- FDA enforcement reports list 1 recall of Draximage Dtpa products; the newest started March 19, 2020. A recall usually concerns specific lots, not every product.
What Draximage Dtpa is
Each Draximage Dtpa product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Kit for the preparation of technetium tc 99M pentetate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| pentetic acid 20 mg injection, powder, lyophilized, for solution (intravenous, respiratory (inhalation)) | Draximage Dtpa | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Kit for the preparation of technetium tc 99M pentetate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA018511 | Jubilant | December 29, 1989 | 1 |
Companies that list Draximage Dtpa
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Draximage Dtpa products.
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
March 19, 2020 · Class II · Terminated · D-1062-2020
Failed Stability Specifications
DRAXIMAGE DTPA (KIT FOR THE PREPARATION OF TECHNETIUM TC 99M PENTETATE INJECTION), 20 mg vial, Rx only, Manufactured for: Jubilant Draximage, Inc., Kirkland, Quebec, Canada, NDC 65174-288-05, 67175-288-30 — Jubilant Draximage Inc
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 labeling (SPL, 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
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.