NDC 61787-515 – Diabetic Tussin DM Maximum Strength
Dextromethorphan Hydrobromide 20 mg/10mL; Guaifenesin 400 mg/10mL · Liquid · Oral
Product NDC61787-515
Product details
- Brand name
- Diabetic Tussin DM Maximum Strength
- Generic name
- Dextromethorphan Hydrobromide and Guaifenesin
- Labeler
- MEDTECH PRODUCTS INC
- Dosage form
- Liquid
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- February 1, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Dextromethorphan Hydrobromide 20 mg/10mL
- Guaifenesin 400 mg/10mL
Uses, dosage, side effects and warnings for Diabetic Tussin DM Maximum Strength →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 61787-515-04 | 1 BOTTLE in 1 BOX (61787-515-04) / 118 mL in 1 BOTTLE | Feb 1, 2020 |
| 61787-515-08 | 1 BOTTLE in 1 BOX (61787-515-08) / 237 mL in 1 BOTTLE | Feb 1, 2020 |