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Metoprolol Tartrate

NDC 42708-041, Metoprolol Tartrate, tablet, film coated, from QPharma Inc.

Product NDC
42708-041
Status
Listed
Labeler
QPharma 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/42708-041 \
  -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
42708-041-604270800416060 TABLET, FILM COATED in 1 BOTTLE (42708-041-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ad0606c-7a90-44bd-a75d-d256de30fbcf

Use it

Look up 42708-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-041. 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.