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NDC 42507-192, Fexofenadine Hydrochloride, tablet, from HYVEE INC.

Product NDC
42507-192
Status
Listed
Labeler
HYVEE INC
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/42507-192 \
  -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
42507-192-07425070192071 BOTTLE, PLASTIC in 1 CARTON (42507-192-07) / 60 TABLET in 1 BOTTLE, PLASTIC
42507-192-09425070192091 BOTTLE, PLASTIC in 1 CARTON (42507-192-09) / 90 TABLET in 1 BOTTLE, PLASTIC

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 42507-192 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42507-192 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42507-192. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.