Guaifenesin 71679-0309
Product NDC
71679-0309- Manufacturer
- Health Pharma Usa Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- February 7, 2024
- Listing Expires
- December 31, 2026
- Application
- M012
Active Ingredients
| Ingredient | Strength |
|---|---|
| Guaifenesin | 400 mg/1 |
Drug Class
Expectorant [EPC]Decreased Respiratory Secretion Viscosity [PE]Expectorant [EPC]
Packaging Options(2)
38500 TABLET in 1 BOTTLE (71679-309-00)
200 TABLET in 1 BOTTLE (71679-309-02)