NDC product
POWDER · Teva API India Private Ltd
NDC 15894-0005 · Teva API India Private Ltd
Key facts
| Product NDC | 15894-0005 |
|---|---|
| Nonproprietary name | Quetiapine Fumarate |
| Substances | QUETIAPINE FUMARATE |
| Dosage form | POWDER |
| Labeler | Teva API India Private Ltd |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING |
| Marketing start | Dec 14, 2015 |
| 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: