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metoprolol succinate

NDC 71205-368, metoprolol succinate, tablet, film coated, extended release, from Proficient Rx LP.

Product NDC
71205-368
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204161
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-368 \
  -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
71205-368-307120503683030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-30)
71205-368-607120503686060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-60)
71205-368-907120503689090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/64c65611-d5c9-4802-9edd-32c7c67ce6f4

Use it

Look up 71205-368 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-368 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-368. 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.