Metoprolol succinate
NDC 70518-2080, Metoprolol succinate, tablet, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-2080
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078889
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2080 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METOPROLOL SUCCINATE100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-2080-1 | 70518208001 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2080-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/35304060-0965-488d-9e6e-bd1217286ea1
Use it
Look up 70518-2080 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2080 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2080. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.