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Metoprolol Succinate

NDC 82868-084, Metoprolol Succinate, tablet, film coated, extended release, from Northwind Health Company, LLC.

Product NDC
82868-084
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82868-084 \
  -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 NDCNDC-11Package
82868-084-308286800843030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-30)
82868-084-908286800849090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/471bdbd7-7435-6786-e063-6294a90aa8a0

Use it

Look up 82868-084 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82868-084 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82868-084. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.