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Metoprolol Succinate

NDC 68788-4022, Metoprolol Succinate, tablet, film coated, extended release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4022
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4022 \
  -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
68788-4022-36878840220330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-3)
68788-4022-66878840220660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-6)
68788-4022-96878840220990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/27bb8bd5-b3ae-4eb3-b508-5684904408be

Use it

Look up 68788-4022 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4022 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4022. 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.