NDC Code | 70677-0110-1 |
Package Description | 1 BLISTER PACK in 1 CARTON (70677-0110-1) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 70677-0110 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Guaifenesin And Pseudoephedrine Hcl |
Non-Proprietary Name | Guaifenesin And Pseudoephedrine Hcl |
Dosage Form | TABLET, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20200727 |
Marketing Category Name | ANDA |
Application Number | ANDA208369 |
Manufacturer | Strategic Sourcing Services, LLC |
Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 600; 60 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |