Product NDC: | 49743-3001 |
Proprietary Name: | SelectHealth Tussin DM |
Non Proprietary Name: | Guaifenesin |
Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49743-3001 |
Labeler Name: | Axcentria Pharmaceuticals, LLC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110901 |
Package NDC: | 49743-3001-1 |
Package Description: | 118 mL in 1 BOTTLE (49743-3001-1) |
NDC Code | 49743-3001-1 |
Proprietary Name | SelectHealth Tussin DM |
Package Description | 118 mL in 1 BOTTLE (49743-3001-1) |
Product NDC | 49743-3001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Axcentria Pharmaceuticals, LLC. |
Substance Name | GUAIFENESIN |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |