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Hydrocodone Bitartrate and Acetaminophen - 35356-654-50 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 35356-654
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: 35356-654
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089883
Marketing Category: ANDA
Start Marketing Date: 20120403

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 35356-654-50
Package Description: 50 TABLET in 1 BOTTLE, PLASTIC (35356-654-50)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 35356-654-50
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 50 TABLET in 1 BOTTLE, PLASTIC (35356-654-50)
Product NDC 35356-654
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120403
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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


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