Product NDC: | 59726-480 |
Proprietary Name: | Multi-Symptom NiteTime |
Non Proprietary Name: | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Active Ingredient(s): | 325; 15; 6.25 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59726-480 |
Labeler Name: | P and L Development of New York Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111010 |
Package NDC: | 59726-480-10 |
Package Description: | 1 BOX in 1 BOX (59726-480-10) > 10 CAPSULE, LIQUID FILLED in 1 BOX |
NDC Code | 59726-480-10 |
Proprietary Name | Multi-Symptom NiteTime |
Package Description | 1 BOX in 1 BOX (59726-480-10) > 10 CAPSULE, LIQUID FILLED in 1 BOX |
Product NDC | 59726-480 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20111010 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | P and L Development of New York Corporation |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 325; 15; 6.25 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |