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Hydrocodone Bitartrate And Acetaminophen - 55154-0837-9 - (Hydrocodone Bitartrate And Acetaminophen)

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Drug Information of Hydrocodone Bitartrate And Acetaminophen

Product NDC: 55154-0837
Proprietary Name: Hydrocodone Bitartrate And Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate And Acetaminophen
Active Ingredient(s): 325; 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 Hydrocodone Bitartrate And Acetaminophen

Product NDC: 55154-0837
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040656
Marketing Category: ANDA
Start Marketing Date: 20060119

Package Information of Hydrocodone Bitartrate And Acetaminophen

Package NDC: 55154-0837-9
Package Description: 30 TABLET in 1 BLISTER PACK (55154-0837-9)

NDC Information of Hydrocodone Bitartrate And Acetaminophen

NDC Code 55154-0837-9
Proprietary Name Hydrocodone Bitartrate And Acetaminophen
Package Description 30 TABLET in 1 BLISTER PACK (55154-0837-9)
Product NDC 55154-0837
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate And Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060119
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 7.5
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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