NDC product
FULVESTRANT
NDC 70710-1688 · Zydus Pharmaceuticals USA Inc.
Key facts
| Product NDC | 70710-1688 |
|---|---|
| Proprietary name | FULVESTRANT |
| Nonproprietary name | fulvestrant |
| Substances | FULVESTRANT |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR |
| Labeler | Zydus Pharmaceuticals USA Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA215234 |
| Pharmacologic classes | Estrogen Receptor Antagonist [EPC], Estrogen Receptor Antagonists [MoA], Selective Estrogen Receptor Modulators [MoA] |
| Marketing start | Dec 14, 2021 |
| 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: