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Hydrocodone Polistirex and Chlorpheniramine Polistirex - 54868-6196-0 - (Hydrocodone Polistirex and Chlorpheniramine Polistirex)

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Drug Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

Product NDC: 54868-6196
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
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

Product NDC: 54868-6196
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091632
Marketing Category: ANDA
Start Marketing Date: 20101103

Package Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

Package NDC: 54868-6196-0
Package Description: 1 BOTTLE in 1 CARTON (54868-6196-0) > 473 mL in 1 BOTTLE

NDC Information of Hydrocodone Polistirex and Chlorpheniramine Polistirex

NDC Code 54868-6196-0
Proprietary Name Hydrocodone Polistirex and Chlorpheniramine Polistirex
Package Description 1 BOTTLE in 1 CARTON (54868-6196-0) > 473 mL in 1 BOTTLE
Product NDC 54868-6196
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Polistirex and Chlorpheniramine Polistirex
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20101103
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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 Polistirex


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