NDC 0527-1779 - Temozolomide
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
- 0527-1779
- Package NDCs from labels
- 0527-1779-55, 0527-1779-14
- Manufacturer
- Lannett Company, Inc.
- Effective date
- 2016-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Temozolomide - Lannett Company, Inc. | Lannett Company, Inc. | 2016-04-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0527-1779-14 | Temozolomide | 14 in 1 BOTTLE | CAPSULE | 14 | 13 | |
| 0527-1779-55 | Temozolomide | 5 in 1 BOTTLE | CAPSULE | 5 | 13 |
DailyMed Dashboard NDC Coverage#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.