# FOSAMAX

NDC: 78206-135
Generic name: alendronate sodium
Labeler / Manufacturer: Organon LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210601

FDA application: NDA020560

## 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:"78206-135"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=78206-135
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14e931fd-2c5f-4d90-b7db-5980706f4a56