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hydrocodone bitartrate and acetaminophen - 63629-2958-1 - (hydrocodone bitartrate and acetaminophen)

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Drug Information of hydrocodone bitartrate and acetaminophen

Product NDC: 63629-2958
Proprietary Name: hydrocodone bitartrate and acetaminophen
Non Proprietary Name: hydrocodone bitartrate and acetaminophen
Active Ingredient(s): 7.5; 200    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: 63629-2958
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076642
Marketing Category: ANDA
Start Marketing Date: 20090930

Package Information of hydrocodone bitartrate and acetaminophen

Package NDC: 63629-2958-1
Package Description: 20 TABLET in 1 BOTTLE (63629-2958-1)

NDC Information of hydrocodone bitartrate and acetaminophen

NDC Code 63629-2958-1
Proprietary Name hydrocodone bitartrate and acetaminophen
Package Description 20 TABLET in 1 BOTTLE (63629-2958-1)
Product NDC 63629-2958
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydrocodone bitartrate and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090930
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
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 acetaminophen


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