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
- 62011-0070_277a8bf7-fead-7d5d-e063-6294a90aed0d
- Product NDC
- 62011-0070
- Form
- TABLET, SUGAR COATED
- Composition / generic term
- Ibuprofen and Pseudoephedrine Hydrochloride
- Labeler
- Strategic Sourcing Services LLC
- 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 (62011-0070-1) · 62011-0070-1
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 →