Data / Drug companies / Astellas Pharma Inc.
Astellas Pharma Inc.: 5 products in the FDA NDC directory, labeler code 12838
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Astellas Pharma Inc. (labeler code 12838) lists 5 products in the FDA National Drug Code Directory. By type: 4 drugs for further processing, 1 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on May 12, 2023.
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- Labeler code
- 12838
- 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
- Earliest marketing start
- July 22, 2010
- 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 | 4 | 80% |
| Bulk ingredients | 1 | 20% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 4 | 80% |
| Bulk ingredients | 1 | 20% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Granule, for suspension | 2 | 40% |
| Tablet, coated | 1 | 20% |
| Tablet | 1 | 20% |
| Powder | 1 | 20% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Fezolinetant | 12838-3360 | Tablet, coated | Drugs for further processing | May 12, 2023 |
| Gilteritinib fumarate | 12838-1425 | Tablet | Drugs for further processing | November 28, 2018 |
| Tacrolimus | 12838-1330 | Granule, for suspension | Drugs for further processing | May 24, 2018 |
| Tacrolimus | 12838-1230 | Granule, for suspension | Drugs for further processing | May 24, 2018 |
| Tamsulosin hydrochloride | 12838-2788 | Powder | Bulk ingredients | July 22, 2010 |
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.