Product NDC: | 62211-340 |
Proprietary Name: | Nighttime Cold and Flu Relief |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
Active Ingredient(s): | 325; 15; 6.25 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62211-340 |
Labeler Name: | A&Z Pharmaceutical, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110325 |
Package NDC: | 62211-340-09 |
Package Description: | 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (62211-340-09) |
NDC Code | 62211-340-09 |
Proprietary Name | Nighttime Cold and Flu Relief |
Package Description | 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (62211-340-09) |
Product NDC | 62211-340 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20110325 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | A&Z Pharmaceutical, Inc. |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 325; 15; 6.25 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |