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Levocetirizine Dihydrochloride

NDC 71205-210, levocetirizine Dihydrochloride, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-210
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202046
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LEVOCETIRIZINE DIHYDROCHLORIDE5 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
71205-210-307120502103030 TABLET, FILM COATED in 1 BOTTLE (71205-210-30)
71205-210-607120502106060 TABLET, FILM COATED in 1 BOTTLE (71205-210-60)
71205-210-907120502109090 TABLET, FILM COATED in 1 BOTTLE (71205-210-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f10cfe9a-1884-4a65-b827-8fd781fb75c4

Use it

Look up 71205-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-210. 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.