Xodol - 68453-911-10 - (hydrocodone bitartrate and acetaminophen)

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Drug Information of Xodol

Product NDC: 68453-911
Proprietary Name: Xodol
Non Proprietary Name: hydrocodone bitartrate and acetaminophen
Active Ingredient(s): 300; 10    mg/1; mg/1 & nbsp;   hydrocodone bitartrate and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Xodol

Product NDC: 68453-911
Labeler Name: Victory Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040556
Marketing Category: ANDA
Start Marketing Date: 20070214

Package Information of Xodol

Package NDC: 68453-911-10
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (68453-911-10)

NDC Information of Xodol

NDC Code 68453-911-10
Proprietary Name Xodol
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (68453-911-10)
Product NDC 68453-911
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070214
Marketing Category Name ANDA
Labeler Name Victory Pharma, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 300; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Xodol


General Information