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Sunmark cough dm
Sunmark cough dm - 49348-315-84 - (dextromethorphan polistirex)
Drug Information of Sunmark cough dm
| Product NDC: | 49348-315 |
| Proprietary Name: | Sunmark 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) |
Labeler Information of Sunmark cough dm
| Product NDC: | 49348-315 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091135 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120828 |
Package Information of Sunmark cough dm
| Package NDC: | 49348-315-84 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-315-84) > 89 mL in 1 BOTTLE |
NDC Information of Sunmark cough dm
| NDC Code | 49348-315-84 |
| Proprietary Name | Sunmark cough dm |
| Package Description | 1 BOTTLE in 1 CARTON (49348-315-84) > 89 mL in 1 BOTTLE |
| Product NDC | 49348-315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan polistirex |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20120828 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 30 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
