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FEXOFENADINE HYDROCHLORIDE

NDC 0615-8648, FEXOFENADINE HYDROCHLORIDE, tablet, film coated, from NCS HealthCare of KY, LLC dba Vangard Labs.

Product NDC
0615-8648
Status
Listed
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA091567
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8648 \
  -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
0615-8648-390061586483930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8648-39)

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 0615-8648 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8648 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0615-8648. 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.