Product NDC: | 33992-0611 |
Proprietary Name: | Daytime |
Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 33992-0611 |
Labeler Name: | Greenbrier International |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130201 |
Package NDC: | 33992-0611-0 |
Package Description: | 1 BLISTER PACK in 1 CARTON (33992-0611-0) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 33992-0611-0 |
Proprietary Name | Daytime |
Package Description | 1 BLISTER PACK in 1 CARTON (33992-0611-0) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 33992-0611 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20130201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Greenbrier International |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |