FDA NDC Directory · JSON-LD · Markdown
NDC 0093-9703 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA074260 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | CARBIDOPA HYDRATE (25 mg/1) LEVODOPA (250 mg/1) |
| Marketing started | 20231215 |
| Package count | 3 |
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