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NDC 73150-0200-12 UKONIQ 260.2 mg/1 Details
UKONIQ 260.2 mg/1
UKONIQ is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by TG Therapeutics, Inc.. The primary component is UMBRALISIB TOSYLATE.
MedlinePlus Drug Summary
Umbralisib is used to treat marginal zone lymphoma (MZL; a slow growing cancer that begins in a type of white blood cells that normally fight infection) in adults whose cancer has returned or did not respond to a certain type of medication. It is also used to treat follicular lymphoma (FL; a type of cancer that begins in the white blood cells) in adults whose cancer has returned or did not respond to at least three other medications. Umbralisib is in a class of medications called kinase inhibitors. It works by blocking the action of the abnormal protein that signals cancer cells to multiply. This helps stop the spread of cancer cells.
Related Packages: 73150-0200-12Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Umbralisib
Product Information
| NDC | 73150-0200 |
|---|---|
| Product ID | 73150-200_6f6fcaa4-e82f-4850-bf75-b5806f0478af |
| Associated GPIs | 21533080400320 |
| GCN Sequence Number | 081907 |
| GCN Sequence Number Description | umbralisib tosylate TABLET 200 MG ORAL |
| HIC3 | V1Q |
| HIC3 Description | ANTINEOPLASTIC SYSTEMIC ENZYME INHIBITORS |
| GCN | 49168 |
| HICL Sequence Number | 047104 |
| HICL Sequence Number Description | UMBRALISIB TOSYLATE |
| Brand/Generic | Brand |
| Proprietary Name | UKONIQ |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | umbralisib |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 260.2 |
| Active Ingredient Units | mg/1 |
| Substance Name | UMBRALISIB TOSYLATE |
| Labeler Name | TG Therapeutics, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA213176 |
| Listing Certified Through | 2022-12-31 |
Package
NDC 73150-0200-12 (73150020012)
| NDC Package Code | 73150-200-12 |
|---|---|
| Billing NDC | 73150020012 |
| Package | 4 CARTON in 1 CASE (73150-200-12) / 12 BOTTLE, PLASTIC in 1 CARTON / 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2021-02-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |