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Mucinex
Mucinex - 21695-870-20 - (Guaifenesin)
Drug Information of Mucinex
| Product NDC: | 21695-870 |
| Proprietary Name: | Mucinex |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 600 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex
| Product NDC: | 21695-870 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021282 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090327 |
Package Information of Mucinex
| Package NDC: | 21695-870-20 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (21695-870-20) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Mucinex
| NDC Code | 21695-870-20 |
| Proprietary Name | Mucinex |
| Package Description | 2 BLISTER PACK in 1 CARTON (21695-870-20) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 21695-870 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090327 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | GUAIFENESIN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
