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FEXOFENADINE HYDROCHLORIDE

NDC 72090-010, FEXOFENADINE HYDROCHLORIDE, tablet, from Pioneer Life Sciences, LLC.

Product NDC
72090-010
Status
Listed
Labeler
Pioneer Life Sciences, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA210137
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72090-010 \
  -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
72090-010-017209000100190 TABLET in 1 BOTTLE (72090-010-01)
72090-010-0272090001002100 TABLET in 1 BOTTLE (72090-010-02)
72090-010-037209000100350 TABLET in 1 BOTTLE (72090-010-03)
72090-010-0472090001004150 TABLET in 1 BOTTLE (72090-010-04)
72090-010-99720900010991000 TABLET in 1 BOTTLE (72090-010-99)

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 72090-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72090-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72090-010. 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.