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Labetalol Hydrochloride

NDC 55154-0182, Labetalol Hydrochloride, tablet, film coated, from Cardinal Health 107, LLC.

Product NDC
55154-0182
Status
Listed
Labeler
Cardinal Health 107, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209603
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55154-0182 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LABETALOL HYDROCHLORIDE200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
55154-0182-05515401820010 BLISTER PACK in 1 BAG (55154-0182-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d3ca153c-25b2-4506-91bd-bf9d6a4c01fe

Use it

Look up 55154-0182 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55154-0182 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55154-0182. 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.