United States · FDA National Drug Code directory

Guaifenesin

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
0363-0570_46543546-17f6-6061-e063-6294a90a2e18
Product NDC
0363-0570
Form
TABLET
Composition / generic term
Guaifenesin
Labeler
Walgreens
Marketing category
ANDA
Marketing start / end (source format)
20240613
Source listing expiry
20261231

Source-listed ingredients

  • GUAIFENESIN — 1200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 14 TABLET in 1 BLISTER PACK (0363-0570-27) · 0363-0570-27
  • 28 TABLET in 1 BLISTER PACK (0363-0570-28) · 0363-0570-28

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 →