Metoprolol Succinate
NDC 51655-203, Metoprolol succinate, tablet, extended release, from Northwind Health Company, LLC.
- Product NDC
- 51655-203
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204106
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51655-203 \ -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 |
|---|---|---|
| 51655-203-52 | 51655020352 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-203-52) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c213c327-68b7-da5b-e053-2a95a90a4028
Use it
Look up 51655-203 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-203 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-203. 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.