# Albendazole

NDC: 46708-681
Generic name: Albendazole
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240911

FDA application: ANDA215652

## Active ingredients

- ALBENDAZOLE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-681"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-681
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b4945c7-56e9-47ed-a7ac-5078a1a50b85