Product NDC: | 49348-061 |
Proprietary Name: | sunmark nite time |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
Active Ingredient(s): | 650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-061 |
Labeler Name: | Mckesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111121 |
Package NDC: | 49348-061-39 |
Package Description: | 355 mL in 1 BOTTLE (49348-061-39) |
NDC Code | 49348-061-39 |
Proprietary Name | sunmark nite time |
Package Description | 355 mL in 1 BOTTLE (49348-061-39) |
Product NDC | 49348-061 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20111121 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Mckesson |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 650; 30; 12.5 |
Strength Unit | mg/30mL; mg/30mL; mg/30mL |
Pharmaceutical Classes |