TussiCaps - 0095-0054-01 - (hydrocodone polistirex and chlorpheniramine polistirex)

Alphabetical Index


Drug Information of TussiCaps

Product NDC: 0095-0054
Proprietary Name: TussiCaps
Non Proprietary Name: hydrocodone polistirex and chlorpheniramine polistirex
Active Ingredient(s): 4; 5    mg/1; mg/1 & nbsp;   hydrocodone polistirex and chlorpheniramine polistirex
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of TussiCaps

Product NDC: 0095-0054
Labeler Name: ECR Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077273
Marketing Category: ANDA
Start Marketing Date: 20110902

Package Information of TussiCaps

Package NDC: 0095-0054-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0095-0054-01)

NDC Information of TussiCaps

NDC Code 0095-0054-01
Proprietary Name TussiCaps
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0095-0054-01)
Product NDC 0095-0054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone polistirex and chlorpheniramine polistirex
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110902
Marketing Category Name ANDA
Labeler Name ECR Pharmaceuticals
Substance Name CHLORPHENIRAMINE; HYDROCODONE
Strength Number 4; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of TussiCaps


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