# Alendronate Sodium

NDC: 16714-631
Generic name: Alendronate Sodium
Labeler / Manufacturer: NorthStar Rx LLC
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:"16714-631"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-631
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4323d3aa-cbb0-41e2-aba7-7a94a0516993