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Labetalol Hydrochloride

NDC 60687-439, Labetalol Hydrochloride, tablet, film coated, from American Health Packaging.

Product NDC
60687-439
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207743
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-439 \
  -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
60687-439-0160687043901100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-439-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-439-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3004aa59-288c-4971-b77b-78789715ef5a

  • NADAC price for package 60687043901

    GET /v1/drugs/nadac/60687043901

Use it

Look up 60687-439 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-439 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-439. 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.