Product NDC: | 0904-5764 |
Proprietary Name: | Major Night Time Multi Symptom |
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: | 0904-5764 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 0904-5764-44 |
Package Description: | 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0904-5764-44) |
NDC Code | 0904-5764-44 |
Proprietary Name | Major Night Time Multi Symptom |
Package Description | 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0904-5764-44) |
Product NDC | 0904-5764 |
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 | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 325; 15; 6.25 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |