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Mucinex D
Mucinex D - 63824-057-18 - (Guaifenesin and Pseudoephedrine Hydrochloride)
Drug Information of Mucinex D
| Product NDC: | 63824-057 |
| Proprietary Name: | Mucinex D |
| Non Proprietary Name: | Guaifenesin and Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 600; 60 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) |
Labeler Information of Mucinex D
| Product NDC: | 63824-057 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021585 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120626 |
Package Information of Mucinex D
| Package NDC: | 63824-057-18 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (63824-057-18) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Mucinex D
| NDC Code | 63824-057-18 |
| Proprietary Name | Mucinex D |
| Package Description | 1 BLISTER PACK in 1 CARTON (63824-057-18) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 63824-057 |
| 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 | 600; 60 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
