Product NDC: | 11822-0384 |
Proprietary Name: | Cough DM |
Non Proprietary Name: | dextromethorphan polistirex |
Active Ingredient(s): | 30 mg/5mL & nbsp; dextromethorphan polistirex |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-0384 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA091135 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120827 |
Package NDC: | 11822-0384-1 |
Package Description: | 1 BOTTLE in 1 CARTON (11822-0384-1) > 89 mL in 1 BOTTLE |
NDC Code | 11822-0384-1 |
Proprietary Name | Cough DM |
Package Description | 1 BOTTLE in 1 CARTON (11822-0384-1) > 89 mL in 1 BOTTLE |
Product NDC | 11822-0384 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan polistirex |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20120827 |
Marketing Category Name | ANDA |
Labeler Name | Rite Aid Corporation |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 30 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |