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Metoprolol Tartrate

NDC 72789-583, metoprolol tartrate, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-583
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076704
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-583 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METOPROLOL TARTRATE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-583-307278905833030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-583-30)
72789-583-607278905836060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-583-60)
72789-583-907278905839090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-583-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cbcec1e7-7eac-456e-a253-aaf6761b4883

Use it

Look up 72789-583 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-583 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-583. 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.