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Cetirizine Hydrochloride

NDC 43598-183, Cetirizine Hydrochloride Tablets, tablet, film coated, from Dr. Reddy's Laboratories Inc..

Product NDC
43598-183
Status
Listed
Labeler
Dr. Reddy's Laboratories Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA078343
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-183 \
  -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
43598-183-3143598018331300 TABLET, FILM COATED in 1 BOTTLE (43598-183-31)
43598-183-5543598018355500 TABLET, FILM COATED in 1 BOTTLE (43598-183-55)

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 43598-183 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-183 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-183. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.