# Temozolomide

NDC: 82249-404
Generic name: Temozolomide
Labeler / Manufacturer: CivicaScript LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170428

FDA application: ANDA207658

## Active ingredients

- TEMOZOLOMIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82249-404"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82249-404
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56245d21-4a42-471e-bbdc-80b129336e2f