Metoprolol Succinate
NDC 70518-3680, Metoprolol Succinate ER Tablets, tablet, film coated, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-3680
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211143
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3680 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METOPROLOL SUCCINATE50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-3680-1 | 70518368001 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3680-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/28c22fb6-6cc9-4c41-b781-88b33b6c8cee
Use it
Look up 70518-3680 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3680 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3680. 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.