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Leader Allergy Relief D

NDC 70000-0042, Cetirizine hydrochloride, Pseudoephedrine hydrochloride, tablet, film coated, extended release, from Cardinal Health 110, LLC. dba Leader.

Product NDC
70000-0042
Status
Listed
Labeler
Cardinal Health 110, LLC. dba Leader
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA210719
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70000-0042 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CETIRIZINE HYDROCHLORIDE5 mg/1
  • PSEUDOEPHEDRINE HYDROCHLORIDE120 mg/1

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]; alpha-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
70000-0042-17000000420124 BLISTER PACK in 1 CARTON (70000-0042-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 70000004201

    GET /v1/drugs/nadac/70000004201

Use it

Look up 70000-0042 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70000-0042 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70000-0042. 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.