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up and up cough suppressant dm - 11673-384-21 - (dextromethorphan polistirex)

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Drug Information of up and up cough suppressant dm

Product NDC: 11673-384
Proprietary Name: up and up cough suppressant dm
Non Proprietary Name: dextromethorphan polistirex
Active Ingredient(s): 30    mg/5mL & nbsp;   dextromethorphan polistirex
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of up and up cough suppressant dm

Product NDC: 11673-384
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091135
Marketing Category: ANDA
Start Marketing Date: 20121023

Package Information of up and up cough suppressant dm

Package NDC: 11673-384-21
Package Description: 1 BOTTLE in 1 CARTON (11673-384-21) > 89 mL in 1 BOTTLE

NDC Information of up and up cough suppressant dm

NDC Code 11673-384-21
Proprietary Name up and up cough suppressant dm
Package Description 1 BOTTLE in 1 CARTON (11673-384-21) > 89 mL in 1 BOTTLE
Product NDC 11673-384
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextromethorphan polistirex
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20121023
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name DEXTROMETHORPHAN HYDROBROMIDE
Strength Number 30
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of up and up cough suppressant dm


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