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NDC 83324-009, Fexofenadine Hydrochloride, tablet, from Chain Drug Marketing Association, Inc..

Product NDC
83324-009
Status
Listed
Labeler
Chain Drug Marketing Association, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA211075
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83324-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FEXOFENADINE HYDROCHLORIDE60 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
83324-009-12833240009121 BLISTER PACK in 1 CARTON (83324-009-12) / 12 TABLET in 1 BLISTER PACK
83324-009-24833240009242 BLISTER PACK in 1 CARTON (83324-009-24) / 12 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 83324000912

    GET /v1/drugs/nadac/83324000912

  • NADAC price for package 83324000924

    GET /v1/drugs/nadac/83324000924

Use it

Look up 83324-009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83324-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83324-009. 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.