United States · FDA National Drug Code directory

Ibuprofen 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: 51660-423_2f1cab21-cfa7-0b0e-e063-6294a90a9ae6
Product NDC: 51660-423
Form: TABLET, SUGAR COATED
Composition / generic term: ibuprofen and pseudoephedrine hydrochloride
Labeler: Ohm Laboratories Inc.
Marketing category: ANDA
Marketing start / end (source format): 20011013
Source listing expiry: 20261231

Source-listed ingredients

IBUPROFEN — 200 mg/1
PSEUDOEPHEDRINE HYDROCHLORIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

20 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-21) · 51660-423-21
40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-423-41) · 51660-423-41

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 →