Data / Drug companies / Boehringer Ingelheim Pharma GmbH and Co. KG
Boehringer Ingelheim Pharma GmbH and Co. KG: 62 products in the FDA NDC directory, labeler code 12714
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Boehringer Ingelheim Pharma GmbH and Co. KG (labeler code 12714) lists 62 products in the FDA National Drug Code Directory. By type: 33 drugs for further processing, 29 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on October 7, 2025.
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- Labeler code
- 12714
- Products in commercial distribution
- 62
- Packages
- 63
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- December 31, 1981
- 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 | 33 | 53.2% |
| Bulk ingredients | 29 | 46.8% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 33 | 53.2% |
| Bulk ingredients | 29 | 46.8% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 21 | 33.9% |
| Solution | 18 | 29% |
| Tablet | 13 | 21% |
| Liquid | 6 | 9.7% |
| Powder, for solution | 2 | 3.2% |
| Granule | 1 | 1.6% |
| Pellet | 1 | 1.6% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Nerandomilast | 12714-350 | Powder | Bulk ingredients | October 7, 2025 |
| Nerandomilast | 12714-123 | Tablet | Drugs for further processing | October 7, 2025 |
| Nerandomilast | 12714-123 | Tablet | Drugs for further processing | October 7, 2025 |
| Nerandomilast | 12714-122 | Tablet | Drugs for further processing | October 7, 2025 |
| Nerandomilast | 12714-122 | Tablet | Drugs for further processing | October 7, 2025 |
| Zongertinib | 12714-301 | Powder | Bulk ingredients | September 2, 2025 |
| Zongertinib | 12714-128 | Tablet | Drugs for further processing | August 11, 2025 |
| Durvalumab | 12714-087 | Solution | Bulk ingredients | January 1, 2024 |
| Tremelimumab | 12714-104 | Solution | Bulk ingredients | October 21, 2022 |
| Spesolimab | 12714-240 | Liquid | Bulk ingredients | September 1, 2022 |
| Risankizumbab | 12714-216 | Liquid | Bulk ingredients | April 26, 2021 |
| Tafasitamab | 12714-219 | Powder | Drugs for further processing | July 31, 2020 |
| Tafasitamab | 12714-212 | Solution | Bulk ingredients | July 31, 2020 |
| Trastuzumab | 12714-235 | Solution | Bulk ingredients | November 3, 2019 |
| Rituximab | 12714-214 | Solution | Bulk ingredients | July 23, 2019 |
| Risankizumbab | 12714-217 | Solution | Drugs for further processing | April 23, 2019 |
| Risankizumbab | 12714-215 | Liquid | Bulk ingredients | April 23, 2019 |
| Butylscopolamine bromide | 12714-011 | Powder | Bulk ingredients | January 1, 2019 |
| Infliximab | 12714-088 | Solution | Bulk ingredients | December 13, 2017 |
| Pembrolizumab | 12714-091 | Liquid | Drugs for further processing | December 1, 2016 |
| Pembrolizumab | 12714-090 | Solution | Drugs for further processing | December 1, 2016 |
| Palivizumab | 12714-232 | Solution | Drugs for further processing | June 24, 2016 |
| Palivizumab | 12714-231 | Solution | Drugs for further processing | June 24, 2016 |
| Empagliflozin | 12714-201 | Powder | Bulk ingredients | February 18, 2016 |
| Idarucizumab | 12714-196 | Liquid | Drugs for further processing | October 21, 2015 |
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.