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Cetirizine Hydrochloride

NDC 0378-3637, cetirizine hydrochloride, tablet, film coated, from Mylan Pharmaceuticals Inc..

Product NDC
0378-3637
Status
Listed
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076677
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0378-3637 \
  -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
0378-3637-0100378363701100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3637-01)
0378-3637-0500378363705500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3637-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 00378363701

    GET /v1/drugs/nadac/00378363701

  • NADAC price for package 00378363705

    GET /v1/drugs/nadac/00378363705

Use it

Look up 0378-3637 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0378-3637 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0378-3637. 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.