NDC 66993-615 - Cesia
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
- 66993-615
- Package NDCs from labels
- 66993-615-28
- Manufacturer
- Prasco Laboratories
- Effective date
- 2009-02-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cesia - Prasco Laboratories | Prasco Laboratories | 2009-02-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 66993-615-28 | EA - Each | 66993-615 | d69503c5-c4a4-430c-bc7a-ebe18ea1bb46 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| 2DE77089-8D80-FFF0-9C67-24EFA70126D9 | FED687F4-1FFA-49EC-92C9-4D09DE17A833 | 2009-02-17 | Boxed warning, Warnings, Adverse reactions | 2DE77089-8D80-FFF0-9C67-24EFA70126D9 FED687F4-1FFA-49EC-92C9-4D09DE17A833 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.