FDA NDC Directory · JSON-LD · Markdown
NDC 37000-459 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE
| Generic name | OMEPRAZOLE MAGNESIUM |
|---|---|
| Labeler / Manufacturer | The Procter & Gamble Manufacturing Company |
| Marketing category | New Drug Application (innovator) · App NDA021229 |
| Dosage form / route | TABLET, DELAYED RELEASE · ORAL |
| Active ingredients | OMEPRAZOLE MAGNESIUM (20 mg/1) |
| Marketing started | 20120815 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).