# ALENDRONATE SODIUM

NDC: 68071-3771
Generic name: Alendronate sodium
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080804

FDA application: ANDA076768

## 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:"68071-3771"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3771
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2baf8516-4148-9007-e063-6394a90a8094