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Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 69842-973, FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE, tablet, extended release, from CVS Pharmacy.

Product NDC
69842-973
Status
Listed
Labeler
CVS Pharmacy
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA090818
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69842-973 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FEXOFENADINE HYDROCHLORIDE60 mg/1
  • PSEUDOEPHEDRINE HYDROCHLORIDE120 mg/1

Pharmacologic classes

Adrenergic alpha-Agonists [MoA]; Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]; alpha-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
69842-973-20698420973201 BLISTER PACK in 1 CARTON (69842-973-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
69842-973-30698420973301 BLISTER PACK in 1 CARTON (69842-973-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

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 69842-973 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69842-973 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69842-973. 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.