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Lexuss 210
Lexuss 210 - 23359-016-16 - (Codeine Phosphate and Chlorpheniramine Maleate)
Drug Information of Lexuss 210
| Product NDC: | 23359-016 |
| Proprietary Name: | Lexuss 210 |
| Non Proprietary Name: | Codeine Phosphate and Chlorpheniramine Maleate |
| Active Ingredient(s): | 2; 10 mg/5mL; mg/5mL & nbsp; Codeine Phosphate and Chlorpheniramine Maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lexuss 210
| Product NDC: | 23359-016 |
| Labeler Name: | Centurion Labs |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090415 |
Package Information of Lexuss 210
| Package NDC: | 23359-016-16 |
| Package Description: | 473 mL in 1 BOTTLE (23359-016-16) |
NDC Information of Lexuss 210
| NDC Code | 23359-016-16 |
| Proprietary Name | Lexuss 210 |
| Package Description | 473 mL in 1 BOTTLE (23359-016-16) |
| Product NDC | 23359-016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Codeine Phosphate and Chlorpheniramine Maleate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090415 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Centurion Labs |
| Substance Name | CHLORPHENIRAMINE MALEATE; CODEINE PHOSPHATE |
| Strength Number | 2; 10 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
