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Levocetirizine Dihydrochloride

NDC 71335-0789, Levocetirizine Dihydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0789
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091264
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0789 \
  -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
71335-0789-17133507890130 TABLET in 1 BOTTLE (71335-0789-1)
71335-0789-27133507890290 TABLET in 1 BOTTLE (71335-0789-2)
71335-0789-37133507890328 TABLET in 1 BOTTLE (71335-0789-3)
71335-0789-47133507890460 TABLET in 1 BOTTLE (71335-0789-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b7bbffcb-5f56-4735-998a-eadd07dfa2cb

Use it

Look up 71335-0789 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0789 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0789. 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.