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Metoprolol Tartrate

NDC 57237-102, Metoprolol Tartrate, tablet, film coated, from Rising Pharma Holdings, Inc..

Product NDC
57237-102
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077739
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57237-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METOPROLOL TARTRATE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
57237-102-0157237010201100 TABLET, FILM COATED in 1 BOTTLE (57237-102-01)
57237-102-99572370102991000 TABLET, FILM COATED in 1 BOTTLE (57237-102-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30b2b576-4939-4903-be59-dbd1624a5eb6

  • NADAC price for package 57237010201

    GET /v1/drugs/nadac/57237010201

  • NADAC price for package 57237010299

    GET /v1/drugs/nadac/57237010299

Use it

Look up 57237-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57237-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57237-102. 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.