Guaifenesin And Pseudoephedrine Hcl 55111-0799
Product NDC
55111-0799- Manufacturer
- Dr. Reddys Laboratories Limited
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 29, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208369
Active Ingredients
| Ingredient | Strength |
|---|---|
| Guaifenesin | 1200 mg/1 |
| Pseudoephedrine Hydrochloride | 120 mg/1 |
Drug Class
Expectorant [EPC]Adrenergic alpha-Agonists [MoA]Decreased Respiratory Secretion Viscosity [PE]
Packaging Options(4)
4 BLISTER PACK in 1 CARTON (55111-799-04) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-799-06)
1 BLISTER PACK in 1 CARTON (55111-799-12) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
2 BLISTER PACK in 1 CARTON (55111-799-24) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
3 BLISTER PACK in 1 CARTON (55111-799-36) / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK