# Alendronate Sodium

NDC: 64980-340
Generic name: Alendronate Sodium
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080804

FDA application: ANDA090124

## Active ingredients

- ALENDRONATE SODIUM: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64980-340"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-340
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ffdd2496-d253-419b-85a6-8c615f7545f1