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Metoprolol succinate

NDC 71765-008, Metoprolol succinate, tablet, extended release, from Zhejiang Jutai Pharamceutical Co., Ltd.

Product NDC
71765-008
Status
Listed
Labeler
Zhejiang Jutai Pharamceutical Co., Ltd
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214110
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71765-008 \
  -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
71765-008-0171765000801100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71765-008-01)
71765-008-02717650008021000 TABLET, EXTENDED RELEASE in 1 BOTTLE (71765-008-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4df90eca-70e3-5c7c-e063-6294a90adc41

Use it

Look up 71765-008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71765-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71765-008. 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.