United States · FDA National Drug Code directory

SUBVENITE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
69102-418_3e1f8823-3330-41e3-a385-3f65d45a1bca
Product NDC
69102-418
Form
SUSPENSION
Composition / generic term
LAMOTRIGINE
Labeler
OWP Pharmaceuticals, Inc.
Marketing category
NDA
Marketing start / end (source format)
20251001
Source listing expiry
20271231

Source-listed ingredients

  • LAMOTRIGINE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 PACKAGE (69102-418-01) / 240 mL in 1 BOTTLE · 69102-418-01
  • 2 BOTTLE in 1 PACKAGE (69102-418-02) / 240 mL in 1 BOTTLE · 69102-418-02

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →