FDA NDC Directory · JSON-LD · Markdown
NDC 69434-013 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Labeler / Manufacturer | Zhejiang Yongtai Pharmaceutical Co., Ltd |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA217022 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | ESOMEPRAZOLE MAGNESIUM (40 mg/1) |
| Marketing started | 20250109 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).