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Childrens Cetirizine Hydrochloride

NDC 51672-2147, Cetirizine Hydrochloride, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2147
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA090182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2147 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CETIRIZINE HYDROCHLORIDE1 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
51672-2147-1516722147011 BOTTLE in 1 CARTON (51672-2147-1) / 240 mL in 1 BOTTLE
51672-2147-8516722147081 BOTTLE in 1 CARTON (51672-2147-8) / 120 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 51672-2147 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2147 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2147. 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.