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Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 46122-694, Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, tablet, film coated, extended release, from AmeriSource Bergen.

Product NDC
46122-694
Status
Listed
Labeler
AmeriSource Bergen
Dosage form
TABLET, FILM COATED, 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/46122-694 \
  -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
46122-694-65461220694653 BLISTER PACK in 1 CARTON (46122-694-65) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 46122069465

    GET /v1/drugs/nadac/46122069465

Use it

Look up 46122-694 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46122-694 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46122-694. 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.