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Labetalol Hydrochloride

NDC 67296-2114, Labetalol Hydrochloride, tablet, film coated, from RedPharm Drug.

Product NDC
67296-2114
Status
Listed
Labeler
RedPharm Drug
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/67296-2114 \
  -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
67296-2114-26729621140221 TABLET, FILM COATED in 1 BOTTLE (67296-2114-2)
67296-2114-66729621140660 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e1b7355-4802-d277-e063-6394a90aef44

Use it

Look up 67296-2114 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2114 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67296-2114. 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.