Drugplain

YUTIQ .18 mg/1

FLUOCINOLONE ACETONIDE · IMPLANT · ANI Pharmaceuticals, Inc.

No Recall History
Plain English

YUTIQ is a implant containing fluocinolone acetonide at .18 mg/1, taken intravitreal. Manufactured by ANI Pharmaceuticals, Inc..

Key Facts

Brand Name
YUTIQ
Generic Name
FLUOCINOLONE ACETONIDE
NDC Code (Product)
68611-180
Manufacturer
ANI Pharmaceuticals, Inc.
Strength
.18 mg/1
Dosage Form
IMPLANT
Route
INTRAVITREAL
Marketing Status
Application #
NDA210331
Drug Class
Corticosteroid [EPC]
Marketing Start
05/17/2023

Recall History

No Recall History

Frequently Asked Questions

What is YUTIQ used for?

YUTIQ contains FLUOCINOLONE ACETONIDE. It is a implant taken intravitreal. Consult your doctor for specific uses.

Is YUTIQ a controlled substance?

YUTIQ is not classified as a controlled substance by the DEA.

What is the generic name for YUTIQ?

The generic name for YUTIQ is FLUOCINOLONE ACETONIDE. There are 11 other brand versions of FLUOCINOLONE ACETONIDE.

What is the NDC code for YUTIQ .18 mg/1?

The NDC (National Drug Code) for YUTIQ .18 mg/1 is 68611-180, listed by ANI Pharmaceuticals, Inc..