NDC 0185-0932-86 - Cyclosporine
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
- 0185-0932
- Requested NDC
- 0185-0932-86
- Package NDCs from labels
- 0185-0932-86, 0185-0932-30
- Manufacturer
- Eon Labs, Inc.
- Effective date
- 2016-03-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CycloSPORINE Capsules USP (Modified) | Eon Labs, Inc. | 2016-03-23 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0185-0932-30 | EA - Each | 0185-0932 | 928fea14-7d57-4e9c-bc5b-6a38a6ff7020 | 1 | 2012-07-24 |
| 0185-0932-86 | EA - Each | 0185-0932 | 03a7577b-b7fa-400c-b94f-969e6f0132f6 | 1 | 2019-07-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CYCLOSPORINE | ACTIVE INGREDIENT | 83HN0GTJ6D | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| CYCLOSPORINE | ACTIVE MOIETY | 83HN0GTJ6D | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| POLYOXYL 40 HYDROGENATED CASTOR OIL | INACTIVE INGREDIENT | 7YC686GQ8F | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| SORBITOL | INACTIVE INGREDIENT | 506T60A25R | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 | |
| TOCOPHERSOLAN | INACTIVE INGREDIENT | O03S90U1F2 | CYCLOSPORINE CAPSULE [EON LABS, INC.] | 19 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.