Product NDC: | 45737-208 |
Proprietary Name: | Biocotron-D |
Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Active Ingredient(s): | 10; 200; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45737-208 |
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: | 45737-208-16 |
Package Description: | 473 mL in 1 BOTTLE (45737-208-16) |
NDC Code | 45737-208-16 |
Proprietary Name | Biocotron-D |
Package Description | 473 mL in 1 BOTTLE (45737-208-16) |
Product NDC | 45737-208 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
Dosage Form Name | SUSPENSION/ 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 | 10; 200; 5 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |