Norco - 68387-236-30 - (Hydrocodone Bitartrate And Acetaminophen)

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Drug Information of Norco

Product NDC: 68387-236
Proprietary Name: Norco
Non Proprietary Name: Hydrocodone Bitartrate And Acetaminophen
Active Ingredient(s): 325; 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: 68387-236
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040099
Marketing Category: ANDA
Start Marketing Date: 20080201

Package Information of Norco

Package NDC: 68387-236-30
Package Description: 30 TABLET in 1 BOTTLE (68387-236-30)

NDC Information of Norco

NDC Code 68387-236-30
Proprietary Name Norco
Package Description 30 TABLET in 1 BOTTLE (68387-236-30)
Product NDC 68387-236
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate And Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080201
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals 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