United States · FDA National Drug Code directory

robafen dm

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
68788-8268_ec855832-654a-4cc0-b8a0-3e6fa0f3fab4
Product NDC
68788-8268
Form
SOLUTION
Composition / generic term
dextromethorphan hydrobromide, guaifenesin
Labeler
Preferred Pharmaceuticals Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20220923
Source listing expiry
20271231

Source-listed ingredients

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

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (68788-8268-1) / 118 mL in 1 BOTTLE · 68788-8268-1

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.

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robafen dm — United States | Molindra Medicines