# Albendazole

NDC: 0115-1701
Generic name: albendazole
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19960611

FDA application: NDA020666

## 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:"0115-1701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-1701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06b5eefc-0b95-4862-b9b6-770063f2adf0