# Alendronate Sodium

NDC: 50090-2322
Generic name: Alendronate Sodium
Labeler / Manufacturer: A-S Medication Solutions
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: 70 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-2322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-2322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70c27a96-70b1-4d2a-959b-89361fd20c37