NDC 70301-2001 - 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
- 70301-2001
- Package NDCs from labels
- 70301-2001-1, 70301-2001-2
- Manufacturer
- OPKO Pharmaceuticals, LLC
- Effective date
- 2026-03-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Temozolomide - OPKO Pharmaceuticals, LLC | OPKO Pharmaceuticals, LLC | 2026-03-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70301-2001-1 | Temozolomide | 1 in 1 PACKET | CAPSULE | 1 | 1 | |
| 70301-2001-1 | Temozolomide | 5 in 1 CARTON | CAPSULE | 5 | 1 | |
| 70301-2001-2 | Temozolomide | 14 in 1 CARTON | CAPSULE | 14 | 1 | |
| 70301-2001-2 | Temozolomide | 1 in 1 PACKET | CAPSULE | 1 | 1 |
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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| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
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| EO HAND SANITIZER Lavender | ALCOHOL | EO Products, LLC | 36b26803-ed48-498f-bc0e-15473495a35a | 2025-11-21 | Warnings | 3K9958V90M |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.