Data / Drug companies / Novo Nordisk Production Ireland Limited
Novo Nordisk Production Ireland Limited: 5 products in the FDA NDC directory, labeler code 56125
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Novo Nordisk Production Ireland Limited (labeler code 56125) lists 5 products in the FDA National Drug Code Directory. By type: 5 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on October 29, 2019.
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- Labeler code
- 56125
- Products in commercial distribution
- 5
- Packages
- 5
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Products with a marketing end date set
- 5
- Earliest marketing start
- August 25, 2000
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Drugs for further processing | 5 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 5 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 2 | 40% |
| Capsule, delayed release | 1 | 20% |
| Suspension | 1 | 20% |
| Powder, for suspension | 1 | 20% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Diroximel fumarate | 56125-700 | Capsule, delayed release | Drugs for further processing | October 29, 2019 |
| Aprepitant | 56125-634 | Powder, for suspension | Drugs for further processing | September 30, 2015 |
| Aprepitant | 56125-633 | Capsule | Drugs for further processing | March 26, 2003 |
| Aprepitant | 56125-632 | Capsule | Drugs for further processing | March 26, 2003 |
| Sirolimus | 56125-800 | Suspension | Drugs for further processing | August 25, 2000 |
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.