Z-TUSS AC is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Magna Pharmaceuticals, Inc.. The primary component is Chlorpheniramine Maleate; Codeine Phosphate.
| Product ID | 58407-920_967c7a47-f5bb-18ab-e053-2a95a90ad530 |
| NDC | 58407-920 |
| Product Type | Human Otc Drug |
| Proprietary Name | Z-TUSS AC |
| Generic Name | Chlorpheniramine Maleate, Codeine Phosphate |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2011-01-11 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Magna Pharmaceuticals, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE |
| Active Ingredient Strength | 2 mg/5mL; mg/5mL |
| DEA Schedule | CV |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2019-01-01 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2011-09-27 |
| Marketing End Date | 2013-09-30 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2011-01-11 |
| Marketing End Date | 2019-09-01 |
| Ingredient | Strength |
|---|---|
| CHLORPHENIRAMINE MALEATE | 2 mg/5mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 60575-212 | Codar | Chlorpheniramine Maleate, Codeine Phosphate |
| 58407-920 | Z-TUSS | Chlorpheniramine Maleate, Codeine Phosphate |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() Z-TUSS 74710522 2033059 Live/Registered |
MAGNA PHAMACEUTICALS, INC. 1995-08-03 |