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

Hydrocodone Bitartrate and Acetaminophen - 10544-203-04 - (Hydrocodone Bitartrate and Acetaminophen)

Alphabetical Index


Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 10544-203
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Active Ingredient(s): 500; 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 Hydrocodone Bitartrate and Acetaminophen

Product NDC: 10544-203
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040729
Marketing Category: ANDA
Start Marketing Date: 20100125

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 10544-203-04
Package Description: 4 TABLET in 1 BOTTLE (10544-203-04)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 10544-203-04
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 4 TABLET in 1 BOTTLE (10544-203-04)
Product NDC 10544-203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100125
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartrate and Acetaminophen


General Information