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Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 0363-2110, Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, tablet, film coated, extended release, from walgreens.

Product NDC
0363-2110
Status
Listed
Labeler
walgreens
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/0363-2110 \
  -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
0363-2110-200036321102020 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-2110-20)
0363-2110-300036321103030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-2110-30)

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 0363-2110 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0363-2110 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0363-2110. 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.