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Labetalol Hydrochloride

NDC 70771-1165, Labetalol Hydrochloride, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1165
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1165 \
  -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
70771-1165-170771116501100 TABLET, FILM COATED in 1 BOTTLE (70771-1165-1)
70771-1165-37077111650330 TABLET, FILM COATED in 1 BOTTLE (70771-1165-3)
70771-1165-570771116505500 TABLET, FILM COATED in 1 BOTTLE (70771-1165-5)
70771-1165-97077111650990 TABLET, FILM COATED in 1 BOTTLE (70771-1165-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a3c0cc1e-1c01-4009-afdc-d35a66546aec

Use it

Look up 70771-1165 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1165 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1165. 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.