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Fexofenadine Hydrochloride

NDC 68016-995, Fexofenadine hydrochloride, tablet, from Chain Drug Consortium, LLC.

Product NDC
68016-995
Status
Listed
Labeler
Chain Drug Consortium, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076502
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68016-995 \
  -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
68016-995-03680160995031 BOTTLE in 1 CARTON (68016-995-03) / 30 TABLET in 1 BOTTLE
68016-995-45680160995451 BOTTLE in 1 CARTON (68016-995-45) / 45 TABLET in 1 BOTTLE

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 68016-995 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68016-995 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68016-995. 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.