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Metoprolol succinate

NDC 70436-202, Metoprolol succinate, tablet, extended release, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-202
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213854
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-202 \
  -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 NDCNDC-11Package
70436-202-0170436020201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-01)
70436-202-0270436020202500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-02)
70436-202-03704360202031000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-202-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c00f99e2-7a88-6f9b-e053-2995a90a6ace

Use it

Look up 70436-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-202. 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.