Reprexain - 16590-276-71 - (Hydrocodone Bitartrate, Ibuprofen)

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Drug Information of Reprexain

Product NDC: 16590-276
Proprietary Name: Reprexain
Non Proprietary Name: Hydrocodone Bitartrate, Ibuprofen
Active Ingredient(s): 10; 200    mg/1; mg/1 & nbsp;   Hydrocodone Bitartrate, Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Reprexain

Product NDC: 16590-276
Labeler Name: Stat Rx USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076642
Marketing Category: ANDA
Start Marketing Date: 20081216

Package Information of Reprexain

Package NDC: 16590-276-71
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (16590-276-71)

NDC Information of Reprexain

NDC Code 16590-276-71
Proprietary Name Reprexain
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (16590-276-71)
Product NDC 16590-276
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate, Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081216
Marketing Category Name ANDA
Labeler Name Stat Rx USA
Substance Name HYDROCODONE BITARTRATE; IBUPROFEN
Strength Number 10; 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 Reprexain


General Information