Norco - 52544-539-01 - (Hydrocodone Bitatrate and Acetaminophen)

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Drug Information of Norco

Product NDC: 52544-539
Proprietary Name: Norco
Non Proprietary Name: Hydrocodone Bitatrate and Acetaminophen
Active Ingredient(s): 325; 10    mg/1; mg/1 & nbsp;   Hydrocodone Bitatrate and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Norco

Product NDC: 52544-539
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040148
Marketing Category: ANDA
Start Marketing Date: 19970214

Package Information of Norco

Package NDC: 52544-539-01
Package Description: 100 TABLET in 1 BOTTLE (52544-539-01)

NDC Information of Norco

NDC Code 52544-539-01
Proprietary Name Norco
Package Description 100 TABLET in 1 BOTTLE (52544-539-01)
Product NDC 52544-539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitatrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970214
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Norco


General Information