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) |
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 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 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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