Data / Drug companies / Ipsen Biopharmaceuticals, Inc.
Ipsen Biopharmaceuticals, Inc.: 17 products in the FDA NDC directory, labeler code 15054
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Ipsen Biopharmaceuticals, Inc. (labeler code 15054) lists 17 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 17 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on June 10, 2024.
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- Labeler code
- 15054
- Products in commercial distribution
- 17
- Packages
- 19
- Finished drugs by generic name
- 7
- Prescription products
- 17
- Over the counter products
- 0
- Flagged as original packager
- 12 of 12 products that carry the flag
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 2
- Earliest marketing start
- January 3, 2006
- 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) | 14 | 82.4% |
| Biologics (BLA) | 3 | 17.6% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 17 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Palovarotene | 5 | 1 |
| Odevixibat | 4 | 1 |
| Lanreotide acetate | 3 | 4 |
| Botulinum toxin type a | 2 | 3 |
| Irinotecan hydrochloride | 1 | 12 |
| Elafibranor | 1 | 1 |
| Mecasermin | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 7 | 41.2% |
| Injection | 3 | 17.6% |
| Injection, powder, lyophilized, for solution | 2 | 11.8% |
| Capsule, coated pellets | 2 | 11.8% |
| Injection, powder, for solution | 1 | 5.9% |
| Tablet, film coated | 1 | 5.9% |
| Injection, solution | 1 | 5.9% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Retinoid | 5 |
| Ileal Bile Acid Transporter Inhibitor | 4 |
| Somatostatin Analog | 3 |
| Acetylcholine Release Inhibitor | 2 |
| Neuromuscular Blocker | 2 |
| Topoisomerase Inhibitor | 1 |
| Peroxisome Proliferator-activated Receptor Agonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Iqirvo | 15054-0080 | Tablet, film coated | New drug applications (NDA) | June 10, 2024 |
| Bylvay | 15054-3304 | Capsule | New drug applications (NDA) | January 10, 2024 |
| Bylvay | 15054-3303 | Capsule, coated pellets | New drug applications (NDA) | January 10, 2024 |
| Bylvay | 15054-3302 | Capsule | New drug applications (NDA) | January 10, 2024 |
| Bylvay | 15054-3301 | Capsule, coated pellets | New drug applications (NDA) | January 10, 2024 |
| Sohonos | 15054-0100 | Capsule | New drug applications (NDA) | August 16, 2023 |
| Sohonos | 15054-0050 | Capsule | New drug applications (NDA) | August 16, 2023 |
| Sohonos | 15054-0025 | Capsule | New drug applications (NDA) | August 16, 2023 |
| Sohonos | 15054-0015 | Capsule | New drug applications (NDA) | August 16, 2023 |
| Sohonos | 15054-0010 | Capsule | New drug applications (NDA) | August 16, 2023 |
| Onivyde | 15054-0043 | Injection, powder, for solution | New drug applications (NDA) | October 22, 2015 |
| Dysport | 15054-0530 | Injection, powder, lyophilized, for solution | Biologics (BLA) | November 2, 2009 |
| Dysport | 15054-0500 | Injection, powder, lyophilized, for solution | Biologics (BLA) | November 2, 2009 |
| Somatuline depot | 15054-1120 | Injection | New drug applications (NDA) | November 14, 2007 |
| Somatuline depot | 15054-1090 | Injection | New drug applications (NDA) | November 14, 2007 |
| Somatuline depot | 15054-1060 | Injection | New drug applications (NDA) | November 14, 2007 |
| Increlex | 15054-1040 | Injection, solution | Biologics (BLA) | January 3, 2006 |
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.