Product NDC: | 43378-104 |
Proprietary Name: | Zodryl AC 50 |
Non Proprietary Name: | Chlorpheniramine Maleate and Codeine Phosphate |
Active Ingredient(s): | 2; 5 mg/5mL; mg/5mL & nbsp; Chlorpheniramine Maleate and Codeine Phosphate |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43378-104 |
Labeler Name: | CodaDose, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090824 |
Package NDC: | 43378-104-08 |
Package Description: | 236 mL in 1 BOTTLE, PLASTIC (43378-104-08) |
NDC Code | 43378-104-08 |
Proprietary Name | Zodryl AC 50 |
Package Description | 236 mL in 1 BOTTLE, PLASTIC (43378-104-08) |
Product NDC | 43378-104 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chlorpheniramine Maleate and Codeine Phosphate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090824 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CodaDose, Inc. |
Substance Name | CHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE |
Strength Number | 2; 5 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |