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Notuss-NXD
Notuss-NXD - 24839-348-16 - (Codeine Phosphate, Pseudoephedrine HCl, Chlorcyclizine HCl)
Drug Information of Notuss-NXD
| Product NDC: | 24839-348 |
| Proprietary Name: | Notuss-NXD |
| Non Proprietary Name: | Codeine Phosphate, Pseudoephedrine HCl, Chlorcyclizine HCl |
| Active Ingredient(s): | 9.375; 10; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Codeine Phosphate, Pseudoephedrine HCl, Chlorcyclizine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Notuss-NXD
| Product NDC: | 24839-348 |
| Labeler Name: | SJ PHARMACEUTICALS, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101103 |
Package Information of Notuss-NXD
| Package NDC: | 24839-348-16 |
| Package Description: | 473 mL in 1 BOTTLE (24839-348-16) |
NDC Information of Notuss-NXD
| NDC Code | 24839-348-16 |
| Proprietary Name | Notuss-NXD |
| Package Description | 473 mL in 1 BOTTLE (24839-348-16) |
| Product NDC | 24839-348 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Codeine Phosphate, Pseudoephedrine HCl, Chlorcyclizine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20101103 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | SJ PHARMACEUTICALS, LLC |
| Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; CODEINE PHOSPHATE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 9.375; 10; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
