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Labetalol hydrochloride

NDC 50090-7156, Labetalol hydrochloride, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-7156
Status
Listed
Labeler
A-S Medication Solutions
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/50090-7156 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LABETALOL HYDROCHLORIDE300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50090-7156-050090715600100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-0)
50090-7156-15009071560190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a007d945-417c-4647-ab03-95ca219d7d38

Use it

Look up 50090-7156 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7156 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7156. 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.