NDC 43598-232 – Guaifenesin and Dextromethorphan HBR
Guaifenesin 1200 mg/1; Dextromethorphan Hydrobromide 60 mg/1 · Tablet, Extended Release · Oral
Product NDC43598-232
Product details
- Brand name
- Guaifenesin and Dextromethorphan HBR
- Generic name
- Guaifenesin and Dextromethorphan HBR
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA217340
- Marketed since
- August 15, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Guaifenesin 1200 mg/1
- Dextromethorphan Hydrobromide 60 mg/1
Uses, dosage, side effects and warnings for Guaifenesin and Dextromethorphan HBr →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 43598-232-37 | 3 BLISTER PACK in 1 CARTON (43598-232-37) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Dec 1, 2023 |
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- 43598-231 Guaifenesin 600 mg/1; Dextromethorphan Hydrobromide 30 mg/1 · Tablet, Extended Release · Dr. Reddy's Laboratories Inc.