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Labetalol Hydrochloride

NDC 42806-327, Labetalol Hydrochloride, tablet, from Epic Pharma, LLC.

Product NDC
42806-327
Status
Listed
Labeler
Epic Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212990
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42806-327 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LABETALOL HYDROCHLORIDE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42806-327-0142806032701100 TABLET in 1 BOTTLE (42806-327-01)
42806-327-0542806032705500 TABLET in 1 BOTTLE (42806-327-05)
42806-327-10428060327101000 TABLET in 1 BOTTLE (42806-327-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b950655d-a9f8-4ace-bb56-0c7abbca231e

Use it

Look up 42806-327 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42806-327 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42806-327. 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.