YUTIQ
- Product NDC
- 71879-136
- 11-digit product format
- 718790136
- Labeler code
- 71879
- Product ID
- 71879-136_9014ab6d-e677-4993-87d3-aa9a8c250e99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluocinolone acetonide
- Dosage form
- IMPLANT
- Route
- INTRAOCULAR
- Labeler
- EyePoint Pharmaceuticals, Inc
- Application
- NDA210331
- Marketing category
- NDA
- Marketing start
- 2018-10-12
- Marketing end
- 0000-00-00
- Substance
- FLUOCINOLONE ACETONIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71879-136 | YUTIQ (FLUOCINOLONE ACETONIDE) IMPLANT [EYEPOINT PHARMACEUTICALS, INC] | 12 | Legacy NDC | 20250125_43ba66d9-653d-48b9-9914-b0a50b68b79a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71879-136-01 | 71879013601 | 1 POUCH in 1 BOX, UNIT-DOSE (71879-136-01) > 1 APPLICATOR in 1 POUCH > 1 IMPLANT in 1 APPLICATOR | 1 pouch | 2018-10-12 | 0000-00-00 | No | No | Current |