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NDC 55292-0320-60 Isturisa 1 mg/1 Details
Isturisa 1 mg/1
Isturisa is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Recordati Rare Diseases, Inc.. The primary component is OSILODROSTAT PHOSPHATE.
Product Information
NDC | 55292-0320 |
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Product ID | 55292-320_10dfb430-b311-4afe-9f28-e8cb47aa629a |
Associated GPIs | 30022060600320 |
GCN Sequence Number | 080814 |
GCN Sequence Number Description | osilodrostat phosphate TABLET 1 MG ORAL |
HIC3 | P1G |
HIC3 Description | ADRENAL STEROID INHIBITORS |
GCN | 47793 |
HICL Sequence Number | 046396 |
HICL Sequence Number Description | OSILODROSTAT PHOSPHATE |
Brand/Generic | Brand |
Proprietary Name | Isturisa |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Osilodrostat |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, COATED |
Route | ORAL |
Active Ingredient Strength | 1 |
Active Ingredient Units | mg/1 |
Substance Name | OSILODROSTAT PHOSPHATE |
Labeler Name | Recordati Rare Diseases, Inc. |
Pharmaceutical Class | Cortisol Synthesis Inhibitor [EPC], Cytochrome P450 11B1 Inhibitors [MoA], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibit |
DEA Schedule | n/a |
Marketing Category | NDA |
Application Number | NDA212801 |
Listing Certified Through | 2024-12-31 |
Package
NDC 55292-0320-60 (55292032060)
NDC Package Code | 55292-320-60 |
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Billing NDC | 55292032060 |
Package | 60 TABLET, COATED in 1 BLISTER PACK (55292-320-60) |
Marketing Start Date | 2020-03-31 |
NDC Exclude Flag | N |
Pricing Information | N/A |