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 |