Product NDC: | 57896-756 |
Proprietary Name: | Guaiasorb DM |
Non Proprietary Name: | Dextromethorphan Hydrobromide and Guaifenesin |
Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide and Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57896-756 |
Labeler Name: | Geri-Care Pharmaceuticals, Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19950905 |
Package NDC: | 57896-756-04 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (57896-756-04) |
NDC Code | 57896-756-04 |
Proprietary Name | Guaiasorb DM |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (57896-756-04) |
Product NDC | 57896-756 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide and Guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19950905 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Geri-Care Pharmaceuticals, Corp |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 10; 100 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |