| 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 |