Data / Drug companies / Wuhan Calmland Pharmaceuticals Co., Ltd.
Wuhan Calmland Pharmaceuticals Co., Ltd.: 7 products in the FDA NDC directory, labeler code 70747
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Wuhan Calmland Pharmaceuticals Co., Ltd. (labeler code 70747) lists 7 products in the FDA National Drug Code Directory. By type: 7 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on May 29, 2026.
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- Labeler code
- 70747
- Products in commercial distribution
- 7
- Packages
- 7
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- July 20, 2021
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 7 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 7 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 6 | 85.7% |
| Tablet, film coated | 1 | 14.3% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Methotrexate disodium | 70747-1007 | Injection | Bulk ingredients | May 29, 2026 |
| Tenofovir alafenamide fumarate | 70747-1006 | Tablet, film coated | Bulk ingredients | October 30, 2024 |
| Decitabine | 70747-1005 | Injection | Bulk ingredients | July 20, 2021 |
| Docetaxel | 70747-1004 | Injection | Bulk ingredients | July 20, 2021 |
| Paclitaxel | 70747-1003 | Injection | Bulk ingredients | July 20, 2021 |
| Pemetrexed disodium hemipentahydrate | 70747-1002 | Injection | Bulk ingredients | July 20, 2021 |
| Pemetrexed disodium heptahydrate | 70747-1001 | Injection | Bulk ingredients | July 20, 2021 |
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.