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Allergy Relief

NDC 72036-292, Fexofenadine Hydrochloride, tablet, from HARRIS TEETER.

Product NDC
72036-292
Status
Listed
Labeler
HARRIS TEETER
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/72036-292 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FEXOFENADINE HYDROCHLORIDE180 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72036-292-03720360292033 BLISTER PACK in 1 CARTON (72036-292-03) / 5 TABLET in 1 BLISTER PACK
72036-292-04720360292041 BOTTLE, PLASTIC in 1 CARTON (72036-292-04) / 30 TABLET in 1 BOTTLE, PLASTIC
72036-292-09720360292091 BOTTLE, PLASTIC in 1 CARTON (72036-292-09) / 90 TABLET in 1 BOTTLE, PLASTIC

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 72036-292 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72036-292 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72036-292. 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.