FDA NDC Directory · JSON-LD · Markdown
NDC 70954-798 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION
| Labeler / Manufacturer | ANI Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA219161 |
| Dosage form / route | POWDER, FOR SUSPENSION · ORAL |
| Active ingredients | OMEPRAZOLE (40 mg/1) SODIUM BICARBONATE (1680 mg/1) |
| Marketing started | 20260115 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).