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 HistoryFrequently 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..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
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