| Product NDC: | 58407-920 |
| Proprietary Name: | Z-TUSS |
| Non Proprietary Name: | Chlorpheniramine Maleate, Codeine Phosphate |
| Active Ingredient(s): | 2; 9 mg/5mL; mg/5mL & nbsp; Chlorpheniramine Maleate, Codeine Phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58407-920 |
| Labeler Name: | Magna Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110111 |
| Package NDC: | 58407-920-10 |
| Package Description: | 10 mL in 1 BOTTLE (58407-920-10) |
| NDC Code | 58407-920-10 |
| Proprietary Name | Z-TUSS |
| Package Description | 10 mL in 1 BOTTLE (58407-920-10) |
| Product NDC | 58407-920 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorpheniramine Maleate, Codeine Phosphate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110111 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Magna Pharmaceuticals, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE |
| Strength Number | 2; 9 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |