NDC 37808-733 – Mucus Relief DM
Guaifenesin 600 mg/1; Dextromethorphan Hydrobromide 30 mg/1 · Tablet, Extended Release · Oral
Product NDC37808-733
Product details
- Brand name
- Mucus Relief DM
- Generic name
- Guaifenesin, Dextromethorphan HBr
- Labeler
- H E B
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209692
- Marketed since
- February 28, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Guaifenesin 600 mg/1
- Dextromethorphan Hydrobromide 30 mg/1
Uses, dosage, side effects and warnings for Mucus Relief DM →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 37808-733-20 | 1 BOTTLE, PLASTIC in 1 BOX (37808-733-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | Feb 28, 2023 |
| 37808-733-40 | 1 BOTTLE, PLASTIC in 1 BOX (37808-733-40) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC | Feb 28, 2023 |
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