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Metoprolol Succinate

NDC 70518-4090, Metoprolol Succinate, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-4090
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207206
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4090 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METOPROLOL TARTRATE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-4090-37051840900330 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4090-3)
70518-4090-47051840900490 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4090-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c1d1726f-75c6-4c07-b5ff-565c4c4ca904

Use it

Look up 70518-4090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4090. 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.