| Product NDC: | 45737-230 |
| Proprietary Name: | Bio-S-Pres |
| Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Active Ingredient(s): | 5; 50; 2.5 mg/mL; mg/mL; mg/mL & nbsp; Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 45737-230 |
| Labeler Name: | Advanced Generic Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130301 |
| Package NDC: | 45737-230-01 |
| Package Description: | 30 mL in 1 BOTTLE (45737-230-01) |
| NDC Code | 45737-230-01 |
| Proprietary Name | Bio-S-Pres |
| Package Description | 30 mL in 1 BOTTLE (45737-230-01) |
| Product NDC | 45737-230 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Advanced Generic Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 5; 50; 2.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |