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
69102-301_15cf4680-04a8-421c-a475-cd753b58b604
Product NDC
69102-301
Form
TABLET
Composition / generic term
LAMOTRIGINE
Labeler
OWP Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20180310
Source listing expiry
20271231

Source-listed ingredients

  • LAMOTRIGINE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (69102-301-01) · 69102-301-01
  • 6600 TABLET in 1 BOTTLE (69102-301-02) · 69102-301-02

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 →