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Fexofenadine Hydrochloride

NDC 58602-878, Fexofenadine Hydrochloride, tablet, film coated, from Aurohealth LLC.

Product NDC
58602-878
Status
Listed
Labeler
Aurohealth LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA202039
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58602-878 \
  -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
58602-878-09586020878091 BOTTLE in 1 CARTON (58602-878-09) / 30 TABLET, FILM COATED in 1 BOTTLE
58602-878-4058602087840500 TABLET, FILM COATED in 1 BOTTLE (58602-878-40)
58602-878-60586020878601 BLISTER PACK in 1 CARTON (58602-878-60) / 5 TABLET, FILM COATED in 1 BLISTER PACK

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 58602-878 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58602-878 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58602-878. 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.