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Cetirizine Hydrochloride

NDC 69206-990, Cetirizine Hydrochloride, solution, from Aventura Pharmaceuticals, LLC.

Product NDC
69206-990
Status
Listed
Labeler
Aventura Pharmaceuticals, LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078876
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69206-990 \
  -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
69206-990-0169206099001120 mL in 1 BOTTLE (69206-990-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aeb73ab9-3b05-4062-a7fd-352cf2094a56

Use it

Look up 69206-990 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69206-990 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69206-990. 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.