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Cetirizine Hydrochloride Tablets, 10 mg

NDC 25000-220, Cetirizine Hydrochloride, tablet, from MARKSANS PHARMA LIMITED.

Product NDC
25000-220
Status
Listed
Labeler
MARKSANS PHARMA LIMITED
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA078933
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25000-220 \
  -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
25000-220-03250000220031 BOTTLE in 1 CARTON (25000-220-03) / 30 TABLET in 1 BOTTLE
25000-220-08250000220081 BOTTLE in 1 CARTON (25000-220-08) / 100 TABLET in 1 BOTTLE
25000-220-14250000220141000 TABLET in 1 BOTTLE (25000-220-14)
25000-220-78250000220781 BLISTER PACK in 1 CARTON (25000-220-78) / 7 TABLET in 1 BLISTER PACK
25000-220-81250000220811 BLISTER PACK in 1 CARTON (25000-220-81) / 14 TABLET in 1 BLISTER PACK

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 25000-220 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25000-220 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25000-220. 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.