NDC Code | 70000-0580-2 |
Package Description | 2 BLISTER PACK in 1 CARTON (70000-0580-2) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 70000-0580 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Guaifenesin D |
Non-Proprietary Name | Guaifenesin And Pseudoephedrine Hydrochloride |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20210506 |
Marketing Category Name | ANDA |
Application Number | ANDA212542 |
Manufacturer | CARDINAL HEALTH 110, LLC. DBA LEADER |
Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 600; 60 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC] |