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Tussin
Tussin - 0113-2310-26 - (Guaifenesin)
Drug Information of Tussin
| Product NDC: | 0113-2310 |
| Proprietary Name: | Tussin |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tussin
| Product NDC: | 0113-2310 |
| Labeler Name: | L Perrigo Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19870715 |
Package Information of Tussin
| Package NDC: | 0113-2310-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (0113-2310-26) > 118 mL in 1 BOTTLE |
NDC Information of Tussin
| NDC Code | 0113-2310-26 |
| Proprietary Name | Tussin |
| Package Description | 1 BOTTLE in 1 CARTON (0113-2310-26) > 118 mL in 1 BOTTLE |
| Product NDC | 0113-2310 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19870715 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | L Perrigo Company |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
