# Alendronate Sodium

NDC: 0115-1681
Generic name: Alendronate Sodium
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080206

FDA application: ANDA075710

## Active ingredients

- ALENDRONATE SODIUM: 70 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-1681"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-1681
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c23fb7fe-c6b9-4f77-bde7-992222b589d3