# SUBVENITE

NDC: 69102-418
Generic name: LAMOTRIGINE
Labeler / Manufacturer: OWP Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20251001

FDA application: NDA218879

## Active ingredients

- LAMOTRIGINE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69102-418"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69102-418
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=022b0913-f683-4af8-a862-f81b315909b2