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Levocetirizine Dihydrochloride

NDC 69367-238, Levocetirizine Dihydrochloride, tablet, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-238
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203646
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-238 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOCETIRIZINE DIHYDROCHLORIDE5 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
69367-238-096936702380990 TABLET in 1 BOTTLE, PLASTIC (69367-238-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/85dcd6c0-7fb2-40b3-b07f-93bab169011d

  • NADAC price for package 69367023809

    GET /v1/drugs/nadac/69367023809

Use it

Look up 69367-238 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-238 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-238. 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.