NDC 63304-106 – Guaifenesin and Dextromethorphan HBr
Guaifenesin 600 mg/1; Dextromethorphan Hydrobromide 30 mg/1 · Tablet, Extended Release · Oral
Product NDC63304-106
Product details
- Brand name
- Guaifenesin and Dextromethorphan HBr
- Generic name
- Guaifenesin and Dextromethorphan HBr
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214781
- Marketed since
- July 1, 2021
- 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 Guaifenesin and Dextromethorphan HBr →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 63304-106-21 | 1 BLISTER PACK in 1 CARTON (63304-106-21) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Jul 1, 2021 |
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