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Metoprolol Tartrate

NDC 52817-358, Metoprolol Tartrate, tablet, film coated, from TruPharma LLC.

Product NDC
52817-358
Status
Listed
Labeler
TruPharma LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200981
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52817-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METOPROLOL TARTRATE37.5 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
52817-358-1052817035810100 TABLET, FILM COATED in 1 PACKAGE (52817-358-10)
52817-358-5052817035850500 TABLET, FILM COATED in 1 PACKAGE (52817-358-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/52c822f2-4a71-4ab2-a470-58074622846a

  • NADAC price for package 52817035810

    GET /v1/drugs/nadac/52817035810

Use it

Look up 52817-358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52817-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52817-358. 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.