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
- 70677-1010_c604326c-44ff-2c88-4d4f-d5279566bf8d
- Product NDC
- 70677-1010
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Strategic Sourcing Services, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220331
- 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
- 4 BLISTER PACK in 1 CARTON (70677-1010-1) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 70677-1010-1
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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