Notuss-NX - 24839-349-16 - (Codeine Phosphate, Chlorcyclizine HCl)

Alphabetical Index


Drug Information of Notuss-NX

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)

Labeler Information of Notuss-NX

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 Information of Notuss-NX

Package NDC: 24839-349-16
Package Description: 473 mL in 1 BOTTLE (24839-349-16)

NDC Information of Notuss-NX

NDC Code 24839-349-16
Proprietary Name Notuss-NX
Package Description 473 mL in 1 BOTTLE (24839-349-16)
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

Complete Information of Notuss-NX


General Information