# Alendronate Sodium

NDC: 0054-0282
Generic name: Alendronate Sodium
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20201030

FDA application: ANDA090520

## Active ingredients

- ALENDRONATE SODIUM: 70 mg/75mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0282"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0282
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c910bb05-279b-4ffa-a867-46f4a0853ed5