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Labetalol Hydrochloride

NDC 0615-8513, Labetalol Hydrochloride, tablet, film coated, from NCS HealthCare of KY, LLC dba Vangard Labs.

Product NDC
0615-8513
Status
Listed
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209603
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8513 \
  -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
0615-8513-390061585133930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8513-39)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30280d40-28df-4c88-93bd-357a7c528906

Use it

Look up 0615-8513 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8513 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0615-8513. 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.