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LEVOCETIRIZINE DIHYDROCHLORIDE

NDC 33342-200, LEVOCETIRIZINE DIHYDROCHLORIDE, tablet, film coated, from Macleods Pharmaceuticals Limited.

Product NDC
33342-200
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205564
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-200 \
  -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
33342-200-073334202000730 TABLET, FILM COATED in 1 BOTTLE (33342-200-07)
33342-200-103334202001090 TABLET, FILM COATED in 1 BOTTLE (33342-200-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a3c06a5-4a9a-4205-8ae7-c58efeb73c58

  • NADAC price for package 33342020010

    GET /v1/drugs/nadac/33342020010

Use it

Look up 33342-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-200. 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.