NOTUSS - 24839-343-16 - (Codeine Phosphate, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of NOTUSS

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)

Labeler Information of NOTUSS

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 Information of NOTUSS

Package NDC: 24839-343-16
Package Description: 473 mL in 1 BOTTLE (24839-343-16)

NDC Information of NOTUSS

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

Complete Information of NOTUSS


General Information