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 |