Product NDC: | 45737-249 |
Proprietary Name: | Biocof |
Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL |
Active Ingredient(s): | 20; 400; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45737-249 |
Labeler Name: | Advanced Generic Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120701 |
Package NDC: | 45737-249-16 |
Package Description: | 473 mL in 1 BOTTLE (45737-249-16) |
NDC Code | 45737-249-16 |
Proprietary Name | Biocof |
Package Description | 473 mL in 1 BOTTLE (45737-249-16) |
Product NDC | 45737-249 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Advanced Generic Corporation |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 20; 400; 10 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |