# ALENDRONATE SODIUM

NDC: 70518-1192
Generic name: Alendronate sodium
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180516

FDA application: ANDA076768

## Active ingredients

- ALENDRONATE SODIUM: 35 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-1192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7e470d6-508e-466e-a78d-060bbbc9745c