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Z-TUSS
Z-TUSS - 58407-239-01 - (Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride)
Drug Information of Z-TUSS
| Product NDC: | 58407-239 |
| Proprietary Name: | Z-TUSS |
| Non Proprietary Name: | Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 9; 200; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Z-TUSS
| Product NDC: | 58407-239 |
| Labeler Name: | Magna Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111012 |
Package Information of Z-TUSS
| Package NDC: | 58407-239-01 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (58407-239-01) |
NDC Information of Z-TUSS
| NDC Code | 58407-239-01 |
| Proprietary Name | Z-TUSS |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (58407-239-01) |
| Product NDC | 58407-239 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Codeine Phosphate/Guaifenesin/Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111012 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Magna Pharmaceuticals, Inc. |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 9; 200; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
