Product NDC: | 24839-343 |
Proprietary Name: | NOTUSS |
Non Proprietary Name: | Codeine Phosphate, Phenylephrine Hydrochloride |
Active Ingredient(s): | 10; 10 mg/5mL; mg/5mL & nbsp; Codeine Phosphate, Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24839-343 |
Labeler Name: | SJ Pharmaceuticals, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090716 |
Package NDC: | 24839-343-16 |
Package Description: | 473 mL in 1 BOTTLE (24839-343-16) |
NDC Code | 24839-343-16 |
Proprietary Name | NOTUSS |
Package Description | 473 mL in 1 BOTTLE (24839-343-16) |
Product NDC | 24839-343 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Codeine Phosphate, Phenylephrine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090716 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SJ Pharmaceuticals, LLC |
Substance Name | CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 10; 10 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |