Metoprolol succinate
NDC 82009-114, Metoprolol succinate, tablet, film coated, extended release, from Quallent Pharmaceuticals Health LLC.
- Product NDC
- 82009-114
- Status
- Listed
- Labeler
- Quallent Pharmaceuticals Health LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090617
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82009-114 \ -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 |
|---|---|---|
| 82009-114-05 | 82009011405 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82009-114-05) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/250c2428-c8b0-5156-697a-60cb8a45713cNADAC price for package 82009011405
GET /v1/drugs/nadac/82009011405
Use it
Look up 82009-114 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82009-114 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82009-114. 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.