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Fexofenadine Hydrochloride

NDC 71205-739, fexofenadine hydrochloride, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-739
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA212971
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-739 \
  -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
71205-739-307120507393030 TABLET, FILM COATED in 1 BOTTLE (71205-739-30)
71205-739-607120507396060 TABLET, FILM COATED in 1 BOTTLE (71205-739-60)
71205-739-907120507399090 TABLET, FILM COATED in 1 BOTTLE (71205-739-90)

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 71205-739 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-739 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-739. 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.