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Hydrocodone Bitartrate and Ibuprofen - 35356-804-90 - (Hydrocodone Bitartrate and Ibuprofen)

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Drug Information of Hydrocodone Bitartrate and Ibuprofen

Product NDC: 35356-804
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: 35356-804
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC Care Producst
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076642
Marketing Category: ANDA
Start Marketing Date: 20100218

Package Information of Hydrocodone Bitartrate and Ibuprofen

Package NDC: 35356-804-90
Package Description: 90 TABLET in 1 BOTTLE (35356-804-90)

NDC Information of Hydrocodone Bitartrate and Ibuprofen

NDC Code 35356-804-90
Proprietary Name Hydrocodone Bitartrate and Ibuprofen
Package Description 90 TABLET in 1 BOTTLE (35356-804-90)
Product NDC 35356-804
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100218
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC Care Producst
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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