FDA NDC Directory · JSON-LD · Markdown
NDC 0781-2234 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Labeler / Manufacturer | Sandoz Inc |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA076515 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | OMEPRAZOLE (40 mg/1) |
| Marketing started | 20090121 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).