United States · FDA National Drug Code directory
ALLEGRA-D
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
- 50090-1203_a0388348-fc41-4d13-81ad-d8f25cd154d9
- Product NDC
- 50090-1203
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- fexofenadine hydrochloride and pseudoephedrine hydrochloride
- Labeler
- A-S Medication Solutions
- Marketing category
- NDA
- Marketing start / end (source format)
- 20110303
- 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 (50090-1203-0) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK · 50090-1203-0
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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