FDA NDC Directory · JSON-LD · Markdown
NDC 0480-4076 · HUMAN PRESCRIPTION DRUG · EMULSION
| Labeler / Manufacturer | Teva Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA203880 |
| Dosage form / route | EMULSION · OPHTHALMIC |
| Active ingredients | CYCLOSPORINE (.5 mg/mL) |
| Marketing started | 20251028 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).