United States · FDA National Drug Code directory

Guaifenesin 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
41415-994_a36d0524-b1d7-4daf-a62e-54f63168b0cd
Product NDC
41415-994
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Guaifenesin and Pseudoephedrine Hydrochloride
Labeler
PUBLIX SUPER MARKETS, INC
Marketing category
ANDA
Marketing start / end (source format)
20220407
Source listing expiry
20261231

Source-listed ingredients

  • GUAIFENESIN — 600 mg/1
  • PSEUDOEPHEDRINE HYDROCHLORIDE — 60 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (41415-994-18) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 41415-994-18
  • 2 BLISTER PACK in 1 CARTON (41415-994-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 41415-994-36

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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