Data / Drug companies / Guerbet LLC
Guerbet LLC: 16 products in the FDA NDC directory, labeler code 67684
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Guerbet LLC (labeler code 67684) lists 16 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 15 prescription drugs, 1 bulk ingredients. Its main marketing category is new drug applications (NDA). The newest product started marketing on November 14, 2025.
The request: Watch Guerbet LLC (FDA labeler code 67684): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 67684
- Products in commercial distribution
- 16
- Packages
- 44
- Finished drugs by generic name
- 3
- Prescription products
- 15
- Over the counter products
- 0
- Flagged as original packager
- 15 of 15 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- March 20, 2013
- 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) | 15 | 93.8% |
| Bulk ingredients | 1 | 6.2% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 15 | 93.8% |
| Bulk ingredients | 1 | 6.2% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Gadopiclenol | 9 | 2 |
| Gadoterate meglumine | 5 | 4 |
| Ethiodized oil | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 15 | 93.8% |
| Powder | 1 | 6.2% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Gadolinium-based Contrast Agent | 5 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Elucirem | 67684-4251 | Injection | New drug applications (NDA) | November 14, 2025 |
| Elucirem | 67684-4250 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4242 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4241 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4240 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4233 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4232 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4231 | Injection | New drug applications (NDA) | September 21, 2022 |
| Elucirem | 67684-4230 | Injection | New drug applications (NDA) | September 21, 2022 |
| Dotarem | 67684-3001 | Injection | New drug applications (NDA) | September 18, 2019 |
| Ioversol | 67684-8777 | Powder | Bulk ingredients | September 14, 2018 |
| Lipiodol | 67684-1901 | Injection | New drug applications (NDA) | March 21, 2014 |
| Dotarem | 67684-2001 | Injection | New drug applications (NDA) | April 26, 2013 |
| Dotarem | 67684-2000 | Injection | New drug applications (NDA) | April 26, 2013 |
| Dotarem | 67684-2001 | Injection | New drug applications (NDA) | March 20, 2013 |
| Dotarem | 67684-2000 | Injection | New drug applications (NDA) | March 20, 2013 |
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.