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NDC 41520-781, Cetirizine Hydrochloride, tablet, film coated, from American Sales Company.

Product NDC
41520-781
Status
Listed
Labeler
American Sales Company
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA078336
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/41520-781 \
  -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
41520-781-06415200781061 BOTTLE in 1 CARTON (41520-781-06) / 70 TABLET, FILM COATED in 1 BOTTLE
41520-781-39415200781391 BOTTLE in 1 CARTON (41520-781-39) / 30 TABLET, FILM COATED in 1 BOTTLE
41520-781-664152007816614 BLISTER PACK in 1 CARTON (41520-781-66) / 1 TABLET, FILM COATED in 1 BLISTER PACK
41520-781-76415200781761 BOTTLE in 1 CARTON (41520-781-76) / 120 TABLET, FILM COATED 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 41520-781 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/41520-781 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 41520-781. 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.