Home > National Drug Code (NDC) > Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate and Acetaminophen - 0121-0655-04 - (HYDROCODONE BITARTRATE and ACETAMINOPHEN)

Alphabetical Index


Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 0121-0655
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: HYDROCODONE BITARTRATE and ACETAMINOPHEN
Active Ingredient(s): 167; 2.5    mg/5mL; mg/5mL & nbsp;   HYDROCODONE BITARTRATE and ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 0121-0655
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040182
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 0121-0655-04
Package Description: 118 mL in 1 BOTTLE (0121-0655-04)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 0121-0655-04
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 118 mL in 1 BOTTLE (0121-0655-04)
Product NDC 0121-0655
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE and ACETAMINOPHEN
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 167; 2.5
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartrate and Acetaminophen


General Information