Data / Drug companies / Tianjin Tianyao Pharmaceuticals Co., Ltd.
Tianjin Tianyao Pharmaceuticals Co., Ltd.: 20 products in the FDA NDC directory, labeler code 57582
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Tianjin Tianyao Pharmaceuticals Co., Ltd. (labeler code 57582) lists 20 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 11 bulk ingredients, 5 prescription drugs. Its main marketing category is drugs for further processing. The newest product started marketing on May 1, 2025.
The request: Watch Tianjin Tianyao Pharmaceuticals Co., Ltd. (FDA labeler code 57582): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 57582
- Products in commercial distribution
- 20
- Packages
- 28
- Finished drugs by generic name
- 2
- Prescription products
- 5
- Over the counter products
- 0
- Flagged as original packager
- 5 of 5 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- February 1, 2012
- 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 | 8 | 40% |
| Bulk ingredients | 7 | 35% |
| Generic drugs (ANDA) | 5 | 25% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 11 | 55% |
| Prescription drugs | 5 | 25% |
| Drugs for further processing | 4 | 20% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Celecoxib | 4 | 63 |
| Methylprednisolone | 1 | 31 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 15 | 75% |
| Capsule | 4 | 20% |
| Tablet | 1 | 5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 4 |
| Corticosteroid | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Betamethasone dipropionate | 57582-035 | Powder | Drugs for further processing | May 1, 2025 |
| Betamethasone | 57582-007 | Powder | Bulk ingredients | July 15, 2022 |
| Dexamethasone sodium phosphate | 57582-015 | Powder | Bulk ingredients | January 20, 2022 |
| Trilostane | 57582-041 | Powder | Drugs for further processing | October 1, 2021 |
| Deflazacort | 57582-040 | Powder | Drugs for further processing | June 10, 2021 |
| Methylprednisolone hemisuccinate | 57582-012 | Powder | Bulk ingredients | June 10, 2021 |
| Dexamethasone | 57582-931 | Powder | Bulk ingredients | June 1, 2021 |
| Hydrocortisone | 57582-013 | Powder | Bulk ingredients | January 20, 2021 |
| Celecoxib | 57582-032 | Powder | Drugs for further processing | December 1, 2020 |
| Celecoxib | 57582-214 | Capsule | Generic drugs (ANDA) | February 25, 2020 |
| Celecoxib | 57582-213 | Capsule | Generic drugs (ANDA) | February 25, 2020 |
| Celecoxib | 57582-212 | Capsule | Generic drugs (ANDA) | February 25, 2020 |
| Celecoxib | 57582-211 | Capsule | Generic drugs (ANDA) | February 25, 2020 |
| Methylprednisolone | 57582-101 | Tablet | Generic drugs (ANDA) | May 14, 2018 |
| Prednisolone | 57582-004 | Powder | Drugs for further processing | February 1, 2017 |
| Methylprednisolone | 57582-011 | Powder | Drugs for further processing | July 1, 2015 |
| Dexamethasone | 57582-031 | Powder | Bulk ingredients | June 1, 2014 |
| Spironolactone | 57582-030 | Powder | Drugs for further processing | May 20, 2014 |
| Triamcinolone acetonide | 57582-018 | Powder | Bulk ingredients | January 1, 2014 |
| Prednisone | 57582-003 | Powder | Drugs for further processing | February 1, 2012 |
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.