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Cetirizine Hydrochloride

NDC 16571-401, Cetirizine Hydrochloride, tablet, from Rising Pharma Holdings, Inc..

Product NDC
16571-401
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077829
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16571-401 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CETIRIZINE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
16571-401-1016571040110100 TABLET in 1 BOTTLE (16571-401-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 16571040110

    GET /v1/drugs/nadac/16571040110

Use it

Look up 16571-401 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-401 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-401. 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.