NDC product
POWDER · Dr. Reddy's Laboratories Limited
NDC 30007-837 · Dr. Reddy's Laboratories Limited
Key facts
| Product NDC | 30007-837 |
|---|---|
| Nonproprietary name | TESTOSTERONE EP-USP |
| Substances | TESTOSTERONE |
| Dosage form | POWDER |
| Labeler | Dr. Reddy's Laboratories Limited |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| DEA schedule | CIII |
| Marketing start | Jan 31, 2010 |
| 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: