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NDC 80725-140, Carvedilol, tablet, film coated, from Waylis Therapeutics LLC.

Product NDC
80725-140
Status
Listed
Labeler
Waylis Therapeutics LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020297
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80725-140 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CARVEDILOL6.25 mg/1

Pharmacologic classes

Adrenergic alpha-Antagonists [MoA]; Adrenergic beta1-Antagonists [MoA]; Adrenergic beta2-Antagonists [MoA]; alpha-Adrenergic Blocker [EPC]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
80725-140-2080725014020100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80725-140-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/07c619c6-4a0c-445e-94fa-664a54f68a39

Use it

Look up 80725-140 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80725-140 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80725-140. 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.