Metoprolol Succinate
NDC 67046-0883, Metoprolol Succinate, tablet, extended release, from Coupler LLC.
- Product NDC
- 67046-0883
- Status
- Listed
- Labeler
- Coupler 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/67046-0883 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METOPROLOL SUCCINATE25 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 67046-0883-3 | 67046088303 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-0883-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/55f47fad-ddc9-d9e6-e063-6394a90a48cf
Use it
Look up 67046-0883 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0883 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67046-0883. 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.