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Carvedilol

NDC 70518-0356, Carvedilol, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-0356
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/70518-0356 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CARVEDILOL12.5 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
70518-0356-07051803560030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0356-0)
70518-0356-170518035601180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0356-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/39cf31cc-8f3d-4919-a93a-f997ad6850dc

Use it

Look up 70518-0356 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0356 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0356. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.