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Labetalol Hydrochloride

NDC 67046-1697, Labetalol Hydrochloride, tablet, from Coupler LLC.

Product NDC
67046-1697
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074787
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1697 \
  -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
67046-1697-36704616970330 TABLET in 1 BLISTER PACK (67046-1697-3)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e31f49d-51a1-c509-e063-6294a90a741c

Use it

Look up 67046-1697 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1697 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1697. 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.