# CEVIMELINE

NDC: 69452-316
Generic name: CEVIMELINE HYDROCHLORIDE
Labeler / Manufacturer: Bionpharma Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240117

FDA application: ANDA218290

## 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:"69452-316"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-316
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f15cb50-5917-c928-e063-6294a90ab284