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NDC 36800-691, fexofenadine hydrochloride, tablet, film coated, from Topco Associates LLC.

Product NDC
36800-691
Status
Listed
Labeler
Topco Associates LLC
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/36800-691 \
  -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
36800-691-39368000691391 BOTTLE in 1 CARTON (36800-691-39) / 30 TABLET, FILM COATED in 1 BOTTLE
36800-691-49368000691491 BOTTLE in 1 CARTON (36800-691-49) / 40 TABLET, FILM COATED in 1 BOTTLE
36800-691-75368000691751 BOTTLE in 1 CARTON (36800-691-75) / 90 TABLET, FILM COATED 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 36800-691 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/36800-691 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 36800-691. 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.