Product NDC: | 68016-135 |
Proprietary Name: | Night Time |
Non Proprietary Name: | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Active Ingredient(s): | 325; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68016-135 |
Labeler Name: | Chain Drug Consortium, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120901 |
Package NDC: | 68016-135-00 |
Package Description: | 120 mL in 1 BOTTLE (68016-135-00) |
NDC Code | 68016-135-00 |
Proprietary Name | Night Time |
Package Description | 120 mL in 1 BOTTLE (68016-135-00) |
Product NDC | 68016-135 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120901 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Chain Drug Consortium, LLC |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 325; 15; 6.25 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |