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Labetalol Hydrochloride

NDC 29300-253, Labetalol Hydrochloride, tablet, film coated, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-253
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212719
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-253 \
  -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
29300-253-0129300025301100 TABLET, FILM COATED in 1 BOTTLE (29300-253-01)
29300-253-0529300025305500 TABLET, FILM COATED in 1 BOTTLE (29300-253-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ed0188ba-3fd3-4680-a829-ba242a115fab

Use it

Look up 29300-253 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-253 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-253. 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.