NORCO - 63629-2946-0 - (Hydrocodone bitartrate and acetaminophen)

Alphabetical Index


Drug Information of NORCO

Product NDC: 63629-2946
Proprietary Name: NORCO
Non Proprietary Name: Hydrocodone bitartrate and acetaminophen
Active Ingredient(s): 235; 5    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 NORCO

Product NDC: 63629-2946
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040099
Marketing Category: ANDA
Start Marketing Date: 20090811

Package Information of NORCO

Package NDC: 63629-2946-0
Package Description: 180 TABLET in 1 BOTTLE (63629-2946-0)

NDC Information of NORCO

NDC Code 63629-2946-0
Proprietary Name NORCO
Package Description 180 TABLET in 1 BOTTLE (63629-2946-0)
Product NDC 63629-2946
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090811
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 235; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of NORCO


General Information