NDC product
Arsenic Trioxide
NDC 23155-869 · Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc
Key facts
| Product NDC | 23155-869 |
|---|---|
| Proprietary name | Arsenic Trioxide |
| Nonproprietary name | Arsenic Trioxide |
| Substances | ARSENIC TRIOXIDE |
| Dosage form | INJECTION |
| Route | INTRAVENOUS |
| Labeler | Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA215059 |
| Marketing start | Jun 23, 2023 |
| 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: