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Labetalol hydrochloride

NDC 71205-095, Labetalol hydrochloride, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-095
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075133
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-095 \
  -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
71205-095-307120500953030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-30)
71205-095-607120500956060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60)
71205-095-907120500959090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c0301841-e209-4242-bace-58a20e6dd01b

Use it

Look up 71205-095 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-095 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-095. 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.