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NDC 71879-0136-01 YUTIQ 0.18 mg/1 Details
YUTIQ 0.18 mg/1
YUTIQ is a INTRAOCULAR IMPLANT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by EyePoint Pharmaceuticals, Inc. The primary component is FLUOCINOLONE ACETONIDE.
Product Information
| NDC | 71879-0136 |
|---|---|
| Product ID | 71879-136_0c69de0f-072c-8de5-e063-6294a90a35fe |
| Associated GPIs | 86300017102304 |
| GCN Sequence Number | 079123 |
| GCN Sequence Number Description | fluocinolone acetonide IMPLANT 0.18 MG INTRAOCULR |
| HIC3 | Q6P |
| HIC3 Description | EYE ANTI-INFLAMMATORY AGENTS |
| GCN | 45564 |
| HICL Sequence Number | 002896 |
| HICL Sequence Number Description | FLUOCINOLONE ACETONIDE |
| Brand/Generic | Brand |
| Proprietary Name | YUTIQ |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | fluocinolone acetonide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | IMPLANT |
| Route | INTRAOCULAR |
| Active Ingredient Strength | 0.18 |
| Active Ingredient Units | mg/1 |
| Substance Name | FLUOCINOLONE ACETONIDE |
| Labeler Name | EyePoint Pharmaceuticals, Inc |
| Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA210331 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 71879-0136-01 (71879013601)
| NDC Package Code | 71879-136-01 |
|---|---|
| Billing NDC | 71879013601 |
| Package | 1 POUCH in 1 BOX, UNIT-DOSE (71879-136-01) / 1 APPLICATOR in 1 POUCH / 1 IMPLANT in 1 APPLICATOR |
| Marketing Start Date | 2018-10-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |