Data / Drug companies / Jubilant DraxImage Inc., DBA Jubilant Radiopharma
Jubilant DraxImage Inc., DBA Jubilant Radiopharma: 9 products in the FDA NDC directory, labeler code 65174
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Jubilant DraxImage Inc., DBA Jubilant Radiopharma (labeler code 65174) lists 9 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 9 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on December 4, 2023.
The request: Watch Jubilant DraxImage Inc., DBA Jubilant Radiopharma (FDA labeler code 65174): each new product listing and each discontinued product. $10 of work on sign-up, no card.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Labeler code
- 65174
- Products in commercial distribution
- 9
- Packages
- 11
- Finished drugs by generic name
- 6
- Prescription products
- 9
- Over the counter products
- 0
- Flagged as original packager
- 9 of 9 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- December 30, 1987
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 7 | 77.8% |
| Generic drugs (ANDA) | 1 | 11.1% |
| Biologics (BLA) | 1 | 11.1% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 9 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Sodium iodide i 131 | 2 | 1 |
| Technetium tc 99m sulfur colloid kit | 1 | 1 |
| Technetium tc 99m mertiatide | 1 | 1 |
| Technetium tc 99m medronate | 1 | 2 |
| Rubidium rb 82 | 1 | 1 |
| Kit for the preparation of technetium tc 99m pentetate | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, powder, lyophilized, for solution | 3 | 33.3% |
| Injection, powder, for solution | 2 | 22.2% |
| Kit | 1 | 11.1% |
| Injection, solution | 1 | 11.1% |
| Solution | 1 | 11.1% |
| Capsule | 1 | 11.1% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Radioactive Diagnostic Agent | 2 |
| Radioactive Therapeutic Agent | 2 |
| Lead Chelator | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Kit for the Preparation of Technetium Tc 99m Sulfur Colloid | 65174-179 | Kit | Generic drugs (ANDA) | December 4, 2023 |
| TECHNETIUM Tc 99m MERTIATIDE | 65174-261 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | March 31, 2023 |
| Drax Exametazime | 65174-200 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | August 17, 2017 |
| Ruby-fill | 65174-021 | Injection, solution | New drug applications (NDA) | September 30, 2016 |
| Sodium Iodide I 131 Diagnostic | 65174-461 | Capsule | New drug applications (NDA) | May 1, 2006 |
| Technetium Tc 99m Medronate | 65174-660 | Injection, powder, for solution | New drug applications (NDA) | February 27, 2004 |
| Hicon | 65174-880 | Solution | New drug applications (NDA) | April 7, 2003 |
| Draximage dtpa | 65174-288 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | December 29, 1989 |
| Draximage maa | 65174-270 | Injection, powder, for solution | Biologics (BLA) | December 30, 1987 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.