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Tussin
Tussin - 68016-020-04 - (GUAIFENESIN)
Drug Information of Tussin
| Product NDC: | 68016-020 |
| Proprietary Name: | Tussin |
| 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) |
Labeler Information of Tussin
| Product NDC: | 68016-020 |
| Labeler Name: | Chain Drug Consortium, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120907 |
Package Information of Tussin
| Package NDC: | 68016-020-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (68016-020-04) |
NDC Information of Tussin
| NDC Code | 68016-020-04 |
| Proprietary Name | Tussin |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (68016-020-04) |
| Product NDC | 68016-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120907 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Chain Drug Consortium, LLC |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
