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Fexofenadine hydrochloride

NDC 30142-878, Fexofenadine hydrochloride, tablet, from KROGER COMPANY.

Product NDC
30142-878
Status
Listed
Labeler
KROGER COMPANY
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/30142-878 \
  -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
30142-878-15301420878153 BLISTER PACK in 1 CARTON (30142-878-15) / 5 TABLET in 1 BLISTER PACK
30142-878-30301420878301 BOTTLE in 1 CARTON (30142-878-30) / 30 TABLET in 1 BOTTLE
30142-878-64301420878642 BOTTLE in 1 CARTON (30142-878-64) / 70 TABLET in 1 BOTTLE
30142-878-70301420878701 BOTTLE in 1 CARTON (30142-878-70) / 70 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 30142-878 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/30142-878 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 30142-878. 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.