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metoprolol succinate

NDC 70771-1341, metoprolol succinate, tablet, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1341
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203894
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1341 \
  -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
70771-1341-0707711341001000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1341-0)
70771-1341-170771134101100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1341-1)
70771-1341-570771134105500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1341-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1098f26d-8319-4dba-ad66-3df22db2b399

Use it

Look up 70771-1341 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1341 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1341. 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.