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cetirizine hydrochloride

NDC 68788-4072, Cetirizine Hydrochloride, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4072
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-4072 \
  -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
68788-4072-3687884072031 BOTTLE in 1 CARTON (68788-4072-3) / 30 TABLET, FILM COATED in 1 BOTTLE
68788-4072-66878840720660 TABLET, FILM COATED in 1 BOTTLE (68788-4072-6)
68788-4072-96878840720990 TABLET, FILM COATED in 1 BOTTLE (68788-4072-9)

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 68788-4072 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4072 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4072. 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.