Home
>
National Drug Code (NDC)
>
Sildec PE DM
Sildec PE DM - 21695-900-16 - (Sildec PE DM)
Drug Information of Sildec PE DM
| Product NDC: | 21695-900 |
| Proprietary Name: | Sildec PE DM |
| Non Proprietary Name: | Sildec PE DM |
| Active Ingredient(s): | 4; 15; 12.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Sildec PE DM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sildec PE DM
| Product NDC: | 21695-900 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100331 |
Package Information of Sildec PE DM
| Package NDC: | 21695-900-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (21695-900-16) |
NDC Information of Sildec PE DM
| NDC Code | 21695-900-16 |
| Proprietary Name | Sildec PE DM |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (21695-900-16) |
| Product NDC | 21695-900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sildec PE DM |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20100331 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 15; 12.5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
