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Hydrocodone Polistirex and Chlorpheniramine Polisitrex - 49884-235-33 - (Hydrocodone Polistirex and Chlorpheniramine Polisitrex)

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Drug Information of Hydrocodone Polistirex and Chlorpheniramine Polisitrex

Product NDC: 49884-235
Proprietary Name: Hydrocodone Polistirex and Chlorpheniramine Polisitrex
Non Proprietary Name: Hydrocodone Polistirex and Chlorpheniramine Polisitrex
Active Ingredient(s): 8; 10    mg/5mL; mg/5mL & nbsp;   Hydrocodone Polistirex and Chlorpheniramine Polisitrex
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Polistirex and Chlorpheniramine Polisitrex

Product NDC: 49884-235
Labeler Name: Par Pharmaceutical Companies Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091632
Marketing Category: ANDA
Start Marketing Date: 20120816

Package Information of Hydrocodone Polistirex and Chlorpheniramine Polisitrex

Package NDC: 49884-235-33
Package Description: 473 mL in 1 BOTTLE (49884-235-33)

NDC Information of Hydrocodone Polistirex and Chlorpheniramine Polisitrex

NDC Code 49884-235-33
Proprietary Name Hydrocodone Polistirex and Chlorpheniramine Polisitrex
Package Description 473 mL in 1 BOTTLE (49884-235-33)
Product NDC 49884-235
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Polistirex and Chlorpheniramine Polisitrex
Dosage Form Name SUSPENSION, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120816
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Companies Inc
Substance Name CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE
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 Polisitrex


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