Data / Drug companies / Takeda Pharmaceuticals America, Inc.
Takeda Pharmaceuticals America, Inc.: 19 products in the FDA NDC directory, labeler code 63020
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Takeda Pharmaceuticals America, Inc. (labeler code 63020) lists 19 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 19 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on August 28, 2026.
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- Labeler code
- 63020
- Products in commercial distribution
- 19
- Packages
- 24
- Finished drugs by generic name
- 6
- Prescription products
- 19
- Over the counter products
- 0
- Flagged as original packager
- 14 of 14 products that carry the flag
- Started marketing in the last 12 months
- 5
- Earliest marketing start
- May 13, 2003
- 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) | 19 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 19 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Rusfertide | 5 | 1 |
| Brigatinib | 4 | 1 |
| Ponatinib hydrochloride | 4 | 1 |
| Ixazomib | 3 | 1 |
| Fruquintinib | 2 | 1 |
| Bortezomib | 1 | 26 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 7 | 36.8% |
| Kit | 6 | 31.6% |
| Capsule | 5 | 26.3% |
| Injection, powder, lyophilized, for solution | 1 | 5.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Kinase Inhibitor | 7 |
| Proteasome Inhibitor | 4 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Mimrylo | 63020-765 | Kit | New drug applications (NDA) | August 28, 2026 |
| Mimrylo | 63020-745 | Kit | New drug applications (NDA) | August 28, 2026 |
| Mimrylo | 63020-735 | Kit | New drug applications (NDA) | August 28, 2026 |
| Mimrylo | 63020-725 | Kit | New drug applications (NDA) | August 28, 2026 |
| Mimrylo | 63020-715 | Kit | New drug applications (NDA) | August 28, 2026 |
| Fruzaqla | 63020-225 | Capsule | New drug applications (NDA) | November 8, 2023 |
| Fruzaqla | 63020-210 | Capsule | New drug applications (NDA) | November 8, 2023 |
| Iclusig | 63020-536 | Tablet, film coated | New drug applications (NDA) | January 11, 2021 |
| Alunbrig | 63020-198 | Kit | New drug applications (NDA) | April 28, 2017 |
| Alunbrig | 63020-180 | Tablet, film coated | New drug applications (NDA) | April 28, 2017 |
| Alunbrig | 63020-113 | Tablet, film coated | New drug applications (NDA) | April 28, 2017 |
| Alunbrig | 63020-090 | Tablet, film coated | New drug applications (NDA) | April 28, 2017 |
| Ninlaro | 63020-400 | Capsule | New drug applications (NDA) | November 20, 2015 |
| Ninlaro | 63020-390 | Capsule | New drug applications (NDA) | November 20, 2015 |
| Ninlaro | 63020-230 | Capsule | New drug applications (NDA) | November 20, 2015 |
| Iclusig | 63020-533 | Tablet, film coated | New drug applications (NDA) | April 22, 2015 |
| Iclusig | 63020-535 | Tablet, film coated | New drug applications (NDA) | December 14, 2012 |
| Iclusig | 63020-534 | Tablet, film coated | New drug applications (NDA) | December 14, 2012 |
| Velcade | 63020-049 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | May 13, 2003 |
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.