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Labetalol Hydrochloride

NDC 72162-1677, Labetalol Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
72162-1677
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075215
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1677 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LABETALOL300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72162-1677-172162167701100 TABLET, FILM COATED in 1 BOTTLE (72162-1677-1)
72162-1677-572162167705500 TABLET, FILM COATED in 1 BOTTLE (72162-1677-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f7f7fade-98a6-4741-bfb9-f1eb54ad4565

Use it

Look up 72162-1677 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1677 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1677. 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.