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Carvedilol

NDC 70518-0840, Carvedilol, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-0840
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077614
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0840 \
  -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
70518-0840-27051808400250 POUCH in 1 BOX (70518-0840-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-0840-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6eec3476-f6db-45bd-bb91-4b2d5fbd0f5f

Use it

Look up 70518-0840 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0840 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0840. 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.