Product NDC: | 67510-0521 |
Proprietary Name: | Night Time Gelcap |
Non Proprietary Name: | Acetaminophen, Dextromethorphan, Doxylamine |
Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan, Doxylamine |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67510-0521 |
Labeler Name: | Kareway Product, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110601 |
Package NDC: | 67510-0521-0 |
Package Description: | 2 BLISTER PACK in 1 BOX (67510-0521-0) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 67510-0521-0 |
Proprietary Name | Night Time Gelcap |
Package Description | 2 BLISTER PACK in 1 BOX (67510-0521-0) > 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 67510-0521 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan, Doxylamine |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20110601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kareway Product, Inc. |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 325; 10; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |