Product NDC: | 49348-540 |
Proprietary Name: | sunmark nite time |
Non Proprietary Name: | Dextromethorphan Hydrobromide, Doxylamine Succinate |
Active Ingredient(s): | 15; 6.25 mg/15mL; mg/15mL & nbsp; Dextromethorphan Hydrobromide, Doxylamine Succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-540 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20030703 |
Package NDC: | 49348-540-36 |
Package Description: | 177 mL in 1 BOTTLE (49348-540-36) |
NDC Code | 49348-540-36 |
Proprietary Name | sunmark nite time |
Package Description | 177 mL in 1 BOTTLE (49348-540-36) |
Product NDC | 49348-540 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide, Doxylamine Succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20030703 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 15; 6.25 |
Strength Unit | mg/15mL; mg/15mL |
Pharmaceutical Classes |