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metoprolol succinate

NDC 45963-678, metoprolol succinate, tablet, film coated, extended release, from Actavis Pharma, Inc..

Product NDC
45963-678
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204161
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/45963-678 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METOPROLOL SUCCINATE200 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
45963-678-1145963067811100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-678-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b798601e-a369-4c8b-8235-08900e1b751d

  • NADAC price for package 45963067811

    GET /v1/drugs/nadac/45963067811

Use it

Look up 45963-678 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/45963-678 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 45963-678. 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.