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IDkit HP ONE - 50402-100-22 - (citric acid anhydrous and 13C urea)

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Drug Information of IDkit HP ONE

Product NDC: 50402-100
Proprietary Name: IDkit HP ONE
Non Proprietary Name: citric acid anhydrous and 13C urea
Active Ingredient(s):    & nbsp;   citric acid anhydrous and 13C urea
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of IDkit HP ONE

Product NDC: 50402-100
Labeler Name: Exalenz Bioscience Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021314
Marketing Category: NDA
Start Marketing Date: 20091228

Package Information of IDkit HP ONE

Package NDC: 50402-100-22
Package Description: 5 BOX in 1 CASE (50402-100-22) > 1 KIT in 1 BOX (50402-100-02) * 1 POWDER, FOR SOLUTION in 1 PACKET

NDC Information of IDkit HP ONE

NDC Code 50402-100-22
Proprietary Name IDkit HP ONE
Package Description 5 BOX in 1 CASE (50402-100-22) > 1 KIT in 1 BOX (50402-100-02) * 1 POWDER, FOR SOLUTION in 1 PACKET
Product NDC 50402-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citric acid anhydrous and 13C urea
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20091228
Marketing Category Name NDA
Labeler Name Exalenz Bioscience Ltd.
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Complete Information of IDkit HP ONE


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