Product NDC: | 0363-0934 |
Proprietary Name: | wal tussin dm max |
Non Proprietary Name: | dextromethorphan hbr, guaifenesin |
Active Ingredient(s): | 10; 200 mg/5mL; mg/5mL & nbsp; dextromethorphan hbr, guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0934 |
Labeler Name: | Walgreen Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120119 |
Package NDC: | 0363-0934-26 |
Package Description: | 1 BOTTLE in 1 CARTON (0363-0934-26) > 118 mL in 1 BOTTLE |
NDC Code | 0363-0934-26 |
Proprietary Name | wal tussin dm max |
Package Description | 1 BOTTLE in 1 CARTON (0363-0934-26) > 118 mL in 1 BOTTLE |
Product NDC | 0363-0934 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan hbr, guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120119 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Walgreen Company |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 10; 200 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |