NDC 75929-141 - Retisert
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 75929-141
- Package NDCs from labels
- 75929-141-91
- Manufacturer
- Pharma Packaging Solutions, LLC dba Tjoapack LLC | Bausch and Lomb Ireland Limited
- Effective date
- 2023-08-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Retisert - Pharma Packaging Solutions, LLC dba Tjoapack LLC | Bausch and Lomb Ireland Limited | Pharma Packaging Solutions, LLC dba Tjoapack LLC | Bausch and Lomb Ireland Limited | 2023-08-13 | HUMAN PRESCRIPTION DRUG LABEL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| fluocinolone acetonide | FLUOCINOLONE ACETONIDE | Glenmark Pharmaceuticals Inc., USA | a00224b0-3db5-4d40-b370-5ec5476e1e10 | 2018-12-18 | Adverse reactions | 0CD5FD6S2M |
| FLUOCINOLONE ACETONIDE | FLUOCINOLONE ACETONIDE | Glenmark Pharmaceuticals Inc., USA | 47de7132-c692-4c77-8160-ab0c1f501a7c | 2018-11-01 | Adverse reactions | 0CD5FD6S2M |
| Fluocinolone Acetonide Topical | FLUOCINOLONE ACETONIDE TOPICAL | Actavis Pharma, Inc. | 98dfd7a4-2208-4637-acf5-080a5813a433 | 2016-08-01 | Adverse reactions | 0CD5FD6S2M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.