# ACAMPROSATE CALCIUM

NDC: 70069-860
Generic name: ACAMPROSATE CALCIUM
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260810

FDA application: ANDA218984

## Active ingredients

- ACAMPROSATE CALCIUM: 333 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-860"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-860
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1cfe4675-766f-4f1a-b1a8-96bbdacfcfa5