Product NDC: | 49873-302 |
Proprietary Name: | Stona Cough |
Non Proprietary Name: | dextromethorphan hydrobromide, guaifenesin |
Active Ingredient(s): | 30; 200 mg/10mL; mg/10mL & nbsp; dextromethorphan hydrobromide, guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49873-302 |
Labeler Name: | Sato Pharmaceutical Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20010103 |
Package NDC: | 49873-302-01 |
Package Description: | 1 BOTTLE in 1 CARTON (49873-302-01) > 120 mL in 1 BOTTLE |
NDC Code | 49873-302-01 |
Proprietary Name | Stona Cough |
Package Description | 1 BOTTLE in 1 CARTON (49873-302-01) > 120 mL in 1 BOTTLE |
Product NDC | 49873-302 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan hydrobromide, guaifenesin |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20010103 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Sato Pharmaceutical Co., Ltd. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 30; 200 |
Strength Unit | mg/10mL; mg/10mL |
Pharmaceutical Classes |