Data / Drug companies / AbbVie Ireland NL B.V.
AbbVie Ireland NL B.V.: 23 products in the FDA NDC directory, labeler code 68513
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
AbbVie Ireland NL B.V. (labeler code 68513) lists 23 products in the FDA National Drug Code Directory. By type: 21 drugs for further processing, 2 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on June 27, 2024.
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- Labeler code
- 68513
- Products in commercial distribution
- 23
- Packages
- 23
- 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
- 1
- Earliest marketing start
- September 30, 2011
- 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 | 21 | 91.3% |
| Bulk ingredients | 2 | 8.7% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 21 | 91.3% |
| Bulk ingredients | 2 | 8.7% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 15 | 65.2% |
| Tablet, film coated | 5 | 21.7% |
| Powder | 3 | 13% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Upadacitinib | 68513-2320 | Powder | Bulk ingredients | June 27, 2024 |
| Levothyroxine sodium | 68513-7155 | Powder | Drugs for further processing | June 2, 2023 |
| Upadacitinib | 68513-1043 | Tablet | Drugs for further processing | November 11, 2022 |
| Upadacitinib | 68513-2310 | Tablet | Drugs for further processing | August 7, 2019 |
| Upadacitinib | 68513-2306 | Tablet | Drugs for further processing | August 7, 2019 |
| Elagolix | 68513-0039 | Tablet, film coated | Drugs for further processing | January 22, 2018 |
| Elagolix | 68513-0038 | Tablet, film coated | Drugs for further processing | January 22, 2018 |
| Levothyroxine sodium | 68513-9296 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-7149 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-7148 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-7070 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-7069 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-7068 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-6624 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-6594 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-5182 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-4552 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-4341 | Tablet | Drugs for further processing | November 18, 2016 |
| Levothyroxine sodium | 68513-3727 | Tablet | Drugs for further processing | November 18, 2016 |
| Venetoclax | 68513-0576 | Tablet, film coated | Drugs for further processing | March 21, 2016 |
| Venetoclax | 68513-0566 | Tablet, film coated | Drugs for further processing | March 21, 2016 |
| Venetoclax | 68513-0561 | Tablet, film coated | Drugs for further processing | March 21, 2016 |
| Paricalcitol | 68513-1054 | Powder | Bulk ingredients | September 30, 2011 |
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.