Product NDC: | 41163-010 |
Proprietary Name: | Non Drowsy Cold and Cough PE |
Non Proprietary Name: | Acetaminophen, Dextromathorphan HBr, Gauifenesin, Phenylephrine HCl |
Active Ingredient(s): | 325; 10; 100; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromathorphan HBr, Gauifenesin, Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41163-010 |
Labeler Name: | SUPERVALU INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070222 |
Package NDC: | 41163-010-09 |
Package Description: | 1 BLISTER PACK in 1 CARTON (41163-010-09) > 20 CAPSULE, COATED in 1 BLISTER PACK |
NDC Code | 41163-010-09 |
Proprietary Name | Non Drowsy Cold and Cough PE |
Package Description | 1 BLISTER PACK in 1 CARTON (41163-010-09) > 20 CAPSULE, COATED in 1 BLISTER PACK |
Product NDC | 41163-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromathorphan HBr, Gauifenesin, Phenylephrine HCl |
Dosage Form Name | CAPSULE, COATED |
Route Name | ORAL |
Start Marketing Date | 20070222 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SUPERVALU INC. |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 10; 100; 5 |
Strength Unit | mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes |