United States · FDA National Drug Code directory
Diabetic Tussin DM Maximum Strength
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
- 61787-515_e60166fa-5c2e-4449-9633-97607116cbe5
- Product NDC
- 61787-515
- Form
- LIQUID
- Composition / generic term
- Dextromethorphan Hydrobromide and Guaifenesin
- Labeler
- MEDTECH PRODUCTS INC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200201
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROMETHORPHAN HYDROBROMIDE — 20 mg/10mL
- GUAIFENESIN — 400 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 BOX (61787-515-04) / 118 mL in 1 BOTTLE · 61787-515-04
- 1 BOTTLE in 1 BOX (61787-515-08) / 237 mL in 1 BOTTLE · 61787-515-08
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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