Product NDC: | 24839-349 |
Proprietary Name: | Notuss-NX |
Non Proprietary Name: | Codeine Phosphate, Chlorcyclizine HCl |
Active Ingredient(s): | 9.375; 10 mg/5mL; mg/5mL & nbsp; Codeine Phosphate, Chlorcyclizine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24839-349 |
Labeler Name: | SJ PHARMACEUTICALS, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20101103 |
Package NDC: | 24839-349-10 |
Package Description: | 10 mL in 1 BOTTLE (24839-349-10) |
NDC Code | 24839-349-10 |
Proprietary Name | Notuss-NX |
Package Description | 10 mL in 1 BOTTLE (24839-349-10) |
Product NDC | 24839-349 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Codeine Phosphate, 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 |
Strength Number | 9.375; 10 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |