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Hydrocodone Polistirex and Chlorpheniramine Polistirex - 24486-200-16 - (Hydrocodone Polistirex and Chlorpheniramine Polistirex)

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Drug Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

Product NDC: 24486-200
Proprietary Name: Hydrocodone Polistirex and Chlorpheniramine Polistirex
Non Proprietary Name: Hydrocodone Polistirex and Chlorpheniramine Polistirex
Active Ingredient(s): 8; 10    mg/5mL; mg/5mL & nbsp;   Hydrocodone Polistirex and Chlorpheniramine Polistirex
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

Product NDC: 24486-200
Labeler Name: Aristos Phamaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091671
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

Package NDC: 24486-200-16
Package Description: 473 mL in 1 BOTTLE (24486-200-16)

NDC Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

NDC Code 24486-200-16
Proprietary Name Hydrocodone Polistirex and Chlorpheniramine Polistirex
Package Description 473 mL in 1 BOTTLE (24486-200-16)
Product NDC 24486-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Polistirex and Chlorpheniramine Polistirex
Dosage Form Name SUSPENSION, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Aristos Phamaceuticals, Inc.
Substance Name CHLORPHENIRAMINE; HYDROCODONE
Strength Number 8; 10
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex


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