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Cetirizine Hydrochloride

NDC 51079-597, cetirizine hydrochloride, tablet, film coated, from Mylan Institutional Inc..

Product NDC
51079-597
Status
Listed
Labeler
Mylan Institutional Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076677
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51079-597 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CETIRIZINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51079-597-2051079059720100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-597-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-597-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51079059720

    GET /v1/drugs/nadac/51079059720

Use it

Look up 51079-597 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51079-597 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51079-597. 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.