FDA NDC Directory · JSON-LD · Markdown
NDC 70710-1835 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | levothyroxine sodium |
|---|---|
| Labeler / Manufacturer | Zydus Pharmaceuticals USA Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA217066 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | LEVOTHYROXINE SODIUM ANHYDROUS (500 ug/5mL) |
| Marketing started | 20241101 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).