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Fexofenadine Hydrochloride

NDC 62207-623, Fexofenadine Hydrochloride, tablet, from Granules India Limited.

Product NDC
62207-623
Status
Listed
Labeler
Granules India Limited
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/62207-623 \
  -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
62207-623-416220706234124 TABLET in 1 CONTAINER (62207-623-41)
62207-623-4562207062345225 TABLET in 1 CONTAINER (62207-623-45)
62207-623-576220706235790 TABLET in 1 CONTAINER (62207-623-57)
62207-623-71622070623717 BLISTER PACK in 1 CARTON (62207-623-71) / 10 TABLET 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 62207-623 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62207-623 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62207-623. 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.