NDC product
POWDER · Teva API India Limited
NDC 15894-0039 · Teva API India Limited
Key facts
| Product NDC | 15894-0039 |
|---|---|
| Nonproprietary name | FLUOXETINE hcl |
| Substances | FLUOXETINE HYDROCHLORIDE |
| Dosage form | POWDER |
| Labeler | Teva API India Limited |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Apr 3, 2024 |
| 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: