NDC product
POWDER · Tianjin Pacific Chemical & Pharmaceutical Co., Ltd.
NDC 26251-0005 · Tianjin Pacific Chemical & Pharmaceutical Co., Ltd.
Key facts
| Product NDC | 26251-0005 |
|---|---|
| Nonproprietary name | Trilostane |
| Substances | TRILOSTANE |
| Dosage form | POWDER |
| Labeler | Tianjin Pacific Chemical & Pharmaceutical Co., Ltd. |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Aug 2, 2019 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: