Home
>
National Drug Code (NDC)
>
dextromethorphan polistirex extended release
dextromethorphan polistirex extended release - 45802-433-21 - (dextromethorphan polistirex)
Drug Information of dextromethorphan polistirex extended release
| Product NDC: | 45802-433 |
| Proprietary Name: | dextromethorphan polistirex extended release |
| 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) |
Labeler Information of dextromethorphan polistirex extended release
| Product NDC: | 45802-433 |
| Labeler Name: | Perrigo New York Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091135 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120910 |
Package Information of dextromethorphan polistirex extended release
| Package NDC: | 45802-433-21 |
| Package Description: | 1 BOTTLE in 1 CARTON (45802-433-21) > 89 mL in 1 BOTTLE |
NDC Information of dextromethorphan polistirex extended release
| NDC Code | 45802-433-21 |
| Proprietary Name | dextromethorphan polistirex extended release |
| Package Description | 1 BOTTLE in 1 CARTON (45802-433-21) > 89 mL in 1 BOTTLE |
| Product NDC | 45802-433 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan polistirex |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20120910 |
| Marketing Category Name | ANDA |
| Labeler Name | Perrigo New York Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 30 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
