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LABETALOL HYDROCHLORIDE

NDC 71335-2169, Labetalol Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2169
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211953
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2169 \
  -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
71335-2169-17133521690130 TABLET, FILM COATED in 1 BOTTLE (71335-2169-1)
71335-2169-27133521690290 TABLET, FILM COATED in 1 BOTTLE (71335-2169-2)
71335-2169-37133521690360 TABLET, FILM COATED in 1 BOTTLE (71335-2169-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/04f9dcdf-4023-48ee-9e7d-ca9366d9db72

Use it

Look up 71335-2169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2169. 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.