# cevimeline hydrochloride

NDC: 0713-0937
Generic name: cevimeline hydrochloride
Labeler / Manufacturer: Cosette Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230103

FDA application: NDA020989

## Active ingredients

- CEVIMELINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0713-0937"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0713-0937
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=efc2bb24-4dda-4781-bef5-fcd9abf082dd