Home > National Drug Code (NDC) > HYDROCODONE BITARTRATE AND ACETAMINOPHEN

HYDROCODONE BITARTRATE AND ACETAMINOPHEN - 57664-177-88 - (HYDROCODONE BITARTRATE AND ACETAMINOPHEN)

Alphabetical Index


Drug Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product NDC: 57664-177
Proprietary Name: HYDROCODONE BITARTRATE AND ACETAMINOPHEN
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 HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product NDC: 57664-177
Labeler Name: Caraco Pharmaceutical Laboratories Ltd
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090265
Marketing Category: ANDA
Start Marketing Date: 20110722

Package Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Package NDC: 57664-177-88
Package Description: 100 TABLET in 1 BOTTLE (57664-177-88)

NDC Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN

NDC Code 57664-177-88
Proprietary Name HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Package Description 100 TABLET in 1 BOTTLE (57664-177-88)
Product NDC 57664-177
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110722
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories Ltd
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 HYDROCODONE BITARTRATE AND ACETAMINOPHEN


General Information