Xodol - 42254-301-30 - (hydrocodone bitartrate and acetaminophen)

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Drug Information of Xodol

Product NDC: 42254-301
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: 42254-301
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040556
Marketing Category: ANDA
Start Marketing Date: 20111010

Package Information of Xodol

Package NDC: 42254-301-30
Package Description: 30 TABLET in 1 BOTTLE (42254-301-30)

NDC Information of Xodol

NDC Code 42254-301-30
Proprietary Name Xodol
Package Description 30 TABLET in 1 BOTTLE (42254-301-30)
Product NDC 42254-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111010
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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