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Metoprolol Tartrate

NDC 51655-884, Metoprolol Tartrate, tablet, film coated, from Northwind Health Company, LLC.

Product NDC
51655-884
Status
Listed
Labeler
Northwind Health Company, 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/51655-884 \
  -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
51655-884-525165508845230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-884-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d9df7d01-339c-8985-e053-2a95a90a0d2c

Use it

Look up 51655-884 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-884 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-884. 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.