United States · FDA National Drug Code directory

Loratadine and Pseudoephedrine

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
63187-305_4b42b2f4-a013-4b16-bc3e-d9c3b503beed
Product NDC
63187-305
Form
TABLET, EXTENDED RELEASE
Composition / generic term
loratadine and pseudoephedrine
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20041117
Source listing expiry
20261231

Source-listed ingredients

  • LORATADINE — 10 mg/1
  • PSEUDOEPHEDRINE SULFATE — 240 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (63187-305-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 63187-305-10

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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