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Metoprolol Tartrate

NDC 67296-1903, Metoprolol Tartrate, tablet, film coated, from RedPharm Drug, Inc.

Product NDC
67296-1903
Status
Listed
Labeler
RedPharm Drug, Inc
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/67296-1903 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METOPROLOL TARTRATE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67296-1903-167296190301180 TABLET, FILM COATED in 1 BOTTLE (67296-1903-1)
67296-1903-36729619030330 TABLET, FILM COATED in 1 BOTTLE (67296-1903-3)
67296-1903-66729619030660 TABLET, FILM COATED in 1 BOTTLE (67296-1903-6)
67296-1903-96729619030990 TABLET, FILM COATED in 1 BOTTLE (67296-1903-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=67296-1903

Use it

Look up 67296-1903 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67296-1903 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67296-1903. 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.