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Levocetirizine Dihydrochloride

NDC 0093-7701, Levocetirizine Dihydrochloride, tablet, film coated, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-7701
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090199
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7701 \
  -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
0093-7701-980009377019890 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4f43d057-cba8-4366-86ba-4be361e4c71f

  • NADAC price for package 00093770198

    GET /v1/drugs/nadac/00093770198

Use it

Look up 0093-7701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-7701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-7701. 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.