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FEXOFENADINE HYDROCHLORIDE

NDC 51660-998, FEXOFENADINE HYDROCHLORIDE, tablet, film coated, from OHM LABORATORIES INC..

Product NDC
51660-998
Status
Listed
Labeler
OHM LABORATORIES INC.
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/51660-998 \
  -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
51660-998-30516600998301 BOTTLE in 1 CARTON (51660-998-30) / 30 TABLET, FILM COATED in 1 BOTTLE
51660-998-55516600998551 BOTTLE in 1 CARTON (51660-998-55) / 150 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51660099830

    GET /v1/drugs/nadac/51660099830

  • NADAC price for package 51660099855

    GET /v1/drugs/nadac/51660099855

Use it

Look up 51660-998 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51660-998 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51660-998. 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.