United States · FDA National Drug Code directory

Tussin DM Regular

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
82568-0014_5460ca0d-f6b3-423d-e063-6294a90afce7
Product NDC
82568-0014
Form
LIQUID
Composition / generic term
Dextromethorphan HBr and Guaifenesin
Labeler
AARNA USA, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20250218
Source listing expiry
20271231

Source-listed ingredients

  • DEXTROMETHORPHAN HYDROBROMIDE — 20 mg/10mL
  • GUAIFENESIN — 200 mg/10mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, PLASTIC in 1 PACKAGE (82568-0014-4) / 118 mL in 1 BOTTLE, PLASTIC · 82568-0014-4
  • 473 mL in 1 BOTTLE, PLASTIC (82568-0014-6) · 82568-0014-6
  • 1 BOTTLE, PLASTIC in 1 PACKAGE (82568-0014-8) / 236 mL in 1 BOTTLE, PLASTIC · 82568-0014-8

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 →