United States · FDA National Drug Code directory

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 37808-999_1f6d54d4-f124-4194-b6dc-b9e37fd54faa
Product NDC: 37808-999
Form: TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term: Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler: H E B
Marketing category: ANDA
Marketing start / end (source format): 20180801
Source listing expiry: 20261231

Source-listed ingredients

FEXOFENADINE HYDROCHLORIDE — 60 mg/1
PSEUDOEPHEDRINE HYDROCHLORIDE — 120 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BLISTER PACK in 1 CARTON (37808-999-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 37808-999-30

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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