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MUCINEX
MUCINEX - 55045-3143-2 - (GUAIFENESIN)
Drug Information of MUCINEX
| Product NDC: | 55045-3143 |
| 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: | 55045-3143 |
| Labeler Name: | Dispensing Solutions, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021282 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100512 |
Package Information of MUCINEX
| Package NDC: | 55045-3143-2 |
| Package Description: | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55045-3143-2) |
NDC Information of MUCINEX
| NDC Code | 55045-3143-2 |
| Proprietary Name | MUCINEX |
| Package Description | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55045-3143-2) |
| Product NDC | 55045-3143 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100512 |
| Marketing Category Name | NDA |
| Labeler Name | Dispensing Solutions, Inc. |
| Substance Name | GUAIFENESIN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
