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
0363-6611_95e1422f-6442-48a0-a624-bf10ece0adec
Product NDC
0363-6611
Form
TABLET, EXTENDED RELEASE
Composition / generic term
pseudoephedrine hydrochloride
Labeler
WALGREEN CO.
Marketing category
ANDA
Marketing start / end (source format)
20260130
Source listing expiry
20271231

Source-listed ingredients

  • PSEUDOEPHEDRINE HYDROCHLORIDE — 240 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (0363-6611-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 0363-6611-10

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 →