Product NDC: | 66621-1010 |
Proprietary Name: | ORFADIN |
Non Proprietary Name: | nitisinone |
Active Ingredient(s): | 10 mg/1 & nbsp; nitisinone |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66621-1010 |
Labeler Name: | Rare Disease Therapeutics, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021232 |
Marketing Category: | NDA |
Start Marketing Date: | 20020118 |
Package NDC: | 66621-1010-6 |
Package Description: | 60 CAPSULE in 1 BOTTLE (66621-1010-6) |
NDC Code | 66621-1010-6 |
Proprietary Name | ORFADIN |
Package Description | 60 CAPSULE in 1 BOTTLE (66621-1010-6) |
Product NDC | 66621-1010 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | nitisinone |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20020118 |
Marketing Category Name | NDA |
Labeler Name | Rare Disease Therapeutics, Inc. |
Substance Name | NITISINONE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Hydroxyphenyl-Pyruvate Dioxygenase Inhibitor [EPC],Hydroxyphenylpyruvate Dioxygenase Inhibitors [MoA] |