FDA NDC Directory · JSON-LD · Markdown
NDC 72305-175 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | levothyroxine sodium |
|---|---|
| Labeler / Manufacturer | Provell Pharmaceuticals, LLC |
| Marketing category | New Drug Application (innovator) · App NDA021292 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | LEVOTHYROXINE SODIUM (175 ug/1) |
| Marketing started | 20181017 |
| Marketing ended | 20260831 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).