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Hydrocodone Bitartrate and Ibuprofen - 52959-738-20 - (Hydrocodone Bitartrate and Ibuprofen)

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Drug Information of Hydrocodone Bitartrate and Ibuprofen

Product NDC: 52959-738
Proprietary Name: Hydrocodone Bitartrate and Ibuprofen
Non Proprietary Name: Hydrocodone Bitartrate and Ibuprofen
Active Ingredient(s): 7.5; 200    mg/1; mg/1 & nbsp;   Hydrocodone Bitartrate and Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Ibuprofen

Product NDC: 52959-738
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076642
Marketing Category: ANDA
Start Marketing Date: 20100118

Package Information of Hydrocodone Bitartrate and Ibuprofen

Package NDC: 52959-738-20
Package Description: 20 TABLET in 1 BOTTLE (52959-738-20)

NDC Information of Hydrocodone Bitartrate and Ibuprofen

NDC Code 52959-738-20
Proprietary Name Hydrocodone Bitartrate and Ibuprofen
Package Description 20 TABLET in 1 BOTTLE (52959-738-20)
Product NDC 52959-738
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100118
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name HYDROCODONE BITARTRATE; IBUPROFEN
Strength Number 7.5; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Hydrocodone Bitartrate and Ibuprofen


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