NDC 0002-8980-01 - Rezvoglar KwikPen
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
- 0002-8980
- Requested NDC
- 0002-8980-01
- Package NDCs from labels
- 0002-8980-01, 0002-8980-05
- Manufacturer
- Eli Lilly and Company
- Effective date
- 2024-08-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rezvoglar KwikPen - Eli Lilly and Company | Eli Lilly and Company | 2024-08-09 | HUMAN PRESCRIPTION DRUG LABEL |
| REZVOGLAR KWIKPEN - A-S Medication Solutions | A-S Medication Solutions | 2023-05-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0002-8980-01 | Rezvoglar KwikPen | 3 mL in 1 SYRINGE | INJECTION, SOLUTION | 3 | 7 | |
| 0002-8980-05 | Rezvoglar KwikPen | 5 in 1 CARTON | INJECTION, SOLUTION | 5 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0002-8980-01 | ML - Milliliter | 0002-8980 | adaf4ef0-9f3c-4183-9dba-575e8b82d4a7 | 1 | 2024-11-05 |
| 0002-8980-05 | ML - Milliliter | 0002-8980 | 20369b3b-37de-45eb-9677-ab6bf9dc3a71 | 1 | 2023-04-07 |
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.