Lortab - 50474-910-50 - (hydrocodone bitartrate and acetaminophen)

Alphabetical Index


Drug Information of Lortab

Product NDC: 50474-910
Proprietary Name: Lortab
Non Proprietary Name: hydrocodone bitartrate and acetaminophen
Active Ingredient(s): 500; 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 Lortab

Product NDC: 50474-910
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040100
Marketing Category: ANDA
Start Marketing Date: 19960126

Package Information of Lortab

Package NDC: 50474-910-50
Package Description: 500 TABLET in 1 BOTTLE (50474-910-50)

NDC Information of Lortab

NDC Code 50474-910-50
Proprietary Name Lortab
Package Description 500 TABLET in 1 BOTTLE (50474-910-50)
Product NDC 50474-910
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960126
Marketing Category Name ANDA
Labeler Name UCB, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Lortab


General Information