FDA NDC Directory · JSON-LD · Markdown
NDC 68012-052 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION
| Generic name | omeprazole and sodium bicarbonate |
|---|---|
| Labeler / Manufacturer | Santarus, Inc.. |
| Marketing category | New Drug Application (innovator) · App NDA021636 |
| Dosage form / route | POWDER, FOR SUSPENSION · ORAL |
| Active ingredients | OMEPRAZOLE (20 mg/1) SODIUM BICARBONATE (1680 mg/1) |
| Marketing started | 20040615 |
| Package count | 0 |
Source: openFDA. Public-domain (CC0).