# Albendazole

NDC: 42799-110
Generic name: Albendazole
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190517

FDA application: ANDA211117

## Active ingredients

- ALBENDAZOLE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42799-110"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-110
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c48fd89-cb40-477c-8a78-15cbe0df6faa