Lortab - 54569-0957-1 - (hydrocodone bitartrate and acetaminophen)

Alphabetical Index


Drug Information of Lortab

Product NDC: 54569-0957
Proprietary Name: Lortab
Non Proprietary Name: hydrocodone bitartrate and acetaminophen
Active Ingredient(s): 500; 7.5    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 Lortab

Product NDC: 54569-0957
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089699
Marketing Category: ANDA
Start Marketing Date: 19890825

Package Information of Lortab

Package NDC: 54569-0957-1
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (54569-0957-1)

NDC Information of Lortab

NDC Code 54569-0957-1
Proprietary Name Lortab
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (54569-0957-1)
Product NDC 54569-0957
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19890825
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 7.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Lortab


General Information