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Labetalol Hydrochloride

NDC 71209-084, Labetalol Hydrochloride, tablet, film coated, from Cadila Pharmaceuticals Limited.

Product NDC
71209-084
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211325
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-084 \
  -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
71209-084-037120900840360 TABLET, FILM COATED in 1 BOTTLE (71209-084-03)
71209-084-0571209008405100 TABLET, FILM COATED in 1 BOTTLE (71209-084-05)
71209-084-1071209008410500 TABLET, FILM COATED in 1 BOTTLE (71209-084-10)
71209-084-11712090084111000 TABLET, FILM COATED in 1 BOTTLE (71209-084-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5fba93fc-4580-48c2-a1ec-5d446680adcf

Use it

Look up 71209-084 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-084 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-084. 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.