NDC Code | 68788-7872-3 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7872-3) |
Product NDC | 68788-7872 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Mucus Relief Sinus |
Non-Proprietary Name | Guaifenesin And Phenylephrine Hcl |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20210218 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Application Number | part341 |
Manufacturer | Preferred Pharmaceuticals Inc. |
Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength | 400; 10 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |