# Temozolomide

NDC: 70301-2005
Generic name: TEMOZOLOMIDE
Labeler / Manufacturer: OPKO Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260916

FDA application: ANDA203898

## Active ingredients

- TEMOZOLOMIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70301-2005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70301-2005