Product NDC: | 63824-041 |
Proprietary Name: | Mucinex D |
Non Proprietary Name: | Guaifenesin and Pseudoephedrine Hydrochloride |
Active Ingredient(s): | 1200; 120 mg/1; mg/1 & nbsp; Guaifenesin and Pseudoephedrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63824-041 |
Labeler Name: | Reckitt Benckiser LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021585 |
Marketing Category: | NDA |
Start Marketing Date: | 20120626 |
Package NDC: | 63824-041-71 |
Package Description: | 24 POUCH in 1 CARTON (63824-041-71) > 1 TABLET, EXTENDED RELEASE in 1 POUCH |
NDC Code | 63824-041-71 |
Proprietary Name | Mucinex D |
Package Description | 24 POUCH in 1 CARTON (63824-041-71) > 1 TABLET, EXTENDED RELEASE in 1 POUCH |
Product NDC | 63824-041 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin and Pseudoephedrine Hydrochloride |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20120626 |
Marketing Category Name | NDA |
Labeler Name | Reckitt Benckiser LLC |
Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 1200; 120 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |