# ALENDRONATE SODIUM

NDC: 68788-7130
Generic name: Alendronate sodium
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180330

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:"68788-7130"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7130
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=83e3ba94-d882-4b5c-87cb-af1eb0997efc