NDC 65293-005-00 - Cleviprex
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
- 65293-005
- Requested NDC
- 65293-005-00
- Package NDCs from labels
- 65293-005-50, 65293-005-55, 65293-005-00, 65293-005-11, 65293-005-25, 65293-005-04
- Manufacturer
- The Medicines Company | Fresenius Kabi Austria Graz | Frescinius Kabi Austria Linz
- Effective date
- 2014-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cleviprex - The Medicines Company | Fresenius Kabi Austria Graz | Frescinius Kabi Austria Linz | The Medicines Company | Fresenius Kabi Austria Graz | Frescinius Kabi Austria Linz | 2014-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 65293-005-00 | ML - Milliliter | 65293-005 | 2e2e7f3c-3638-4f96-b2b1-0f505d133f5b | 1 | 2012-07-24 |
| 65293-005-11 | ML - Milliliter | 65293-005 | 958e16a4-d8a9-472f-9549-ffde7e0c978a | 1 | 2013-02-13 |
| 65293-005-50 | ML - Milliliter | 65293-005 | 24131298-04e5-44c3-8c57-1631a06cb93b | 1 | 2012-07-24 |
| 65293-005-55 | ML - Milliliter | 65293-005 | feedcc9d-309a-487e-b82d-79998bf28930 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CLEVIDIPINE | ACTIVE INGREDIENT | 19O2GP3B7Q | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| CLEVIDIPINE | ACTIVE MOIETY | 19O2GP3B7Q | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| EDETATE DISODIUM | INACTIVE INGREDIENT | 7FLD91C86K | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| EGG PHOSPHOLIPIDS | INACTIVE INGREDIENT | 1Z74184RGV | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| OLEIC ACID | INACTIVE INGREDIENT | 2UMI9U37CP | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 | |
| SOYBEAN OIL | INACTIVE INGREDIENT | 241ATL177A | CLEVIPREX (CLEVIDIPINE) EMULSION [THE MEDICINES COMPANY] | 12 |
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.