Data / Drug companies / Taiho Pharmaceutical Co., LTD.
Taiho Pharmaceutical Co., LTD.: 6 products in the FDA NDC directory, labeler code 64842
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Taiho Pharmaceutical Co., LTD. (labeler code 64842) lists 6 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 6 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on June 1, 2026.
The request: Watch Taiho Pharmaceutical Co., LTD. (FDA labeler code 64842): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 64842
- Products in commercial distribution
- 6
- Packages
- 12
- Finished drugs by generic name
- 4
- Prescription products
- 6
- Over the counter products
- 0
- Flagged as original packager
- 6 of 6 products that carry the flag
- Started marketing in the last 12 months
- 2
- Earliest marketing start
- September 22, 2015
- 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) | 6 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 6 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Futibatinib | 2 | 1 |
| Trifluridine and tipiracil | 2 | 1 |
| Lytgobi | 1 | 1 |
| Cedazuridine and decitabine | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 3 | 50% |
| Tablet | 2 | 33.3% |
| Kit | 1 | 16.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nucleoside Metabolic Inhibitor | 3 |
| Kinase Inhibitor | 2 |
| Nucleoside Analog Antiviral | 2 |
| Thymidine Phosphorylase Inhibitor | 2 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Lytgobi | 64842-0128 | Kit | New drug applications (NDA) | June 1, 2026 |
| Lytgobi | 64842-0127 | Tablet | New drug applications (NDA) | June 1, 2026 |
| Lytgobi | 64842-0120 | Tablet | New drug applications (NDA) | February 3, 2023 |
| Inqovi | 64842-0727 | Tablet, film coated | New drug applications (NDA) | July 7, 2020 |
| Lonsurf | 64842-1025 | Tablet, film coated | New drug applications (NDA) | September 22, 2015 |
| Lonsurf | 64842-1020 | Tablet, film coated | New drug applications (NDA) | September 22, 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.