Norco - 52544-913-48 - (Hydrocodone Bitartate and Acetaminophen)

Alphabetical Index


Drug Information of Norco

Product NDC: 52544-913
Proprietary Name: Norco
Non Proprietary Name: Hydrocodone Bitartate and Acetaminophen
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Hydrocodone Bitartate and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Norco

Product NDC: 52544-913
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040099
Marketing Category: ANDA
Start Marketing Date: 19970625

Package Information of Norco

Package NDC: 52544-913-48
Package Description: 4 BLISTER PACK in 1 CARTON (52544-913-48) > 25 TABLET in 1 BLISTER PACK

NDC Information of Norco

NDC Code 52544-913-48
Proprietary Name Norco
Package Description 4 BLISTER PACK in 1 CARTON (52544-913-48) > 25 TABLET in 1 BLISTER PACK
Product NDC 52544-913
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970625
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Norco


General Information