Product NDC: | 49873-306 |
Proprietary Name: | Stona Cough |
Non Proprietary Name: | dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride |
Active Ingredient(s): | 15; 100; 5 mg/1; mg/1; mg/1 & nbsp; dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49873-306 |
Labeler Name: | Sato Pharmaceutical Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20041124 |
Package NDC: | 49873-306-01 |
Package Description: | 1 BOTTLE in 1 CARTON (49873-306-01) > 24 TABLET in 1 BOTTLE |
NDC Code | 49873-306-01 |
Proprietary Name | Stona Cough |
Package Description | 1 BOTTLE in 1 CARTON (49873-306-01) > 24 TABLET in 1 BOTTLE |
Product NDC | 49873-306 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20041124 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Sato Pharmaceutical Co., Ltd. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 15; 100; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |