United States · FDA National Drug Code directory

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
53943-204_0ca9df6b-df27-4658-8c9d-751ceb61d820
Product NDC
53943-204
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Pseudoephedrine hydrochloride
Labeler
DISCOUNT DRUG MART
Marketing category
ANDA
Marketing start / end (source format)
20180302
Source listing expiry
20261231

Source-listed ingredients

  • PSEUDOEPHEDRINE HYDROCHLORIDE — 120 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (53943-204-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 53943-204-10

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →