United States · FDA National Drug Code directory

Lamotrigine

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
49884-882_983458ba-0e97-42af-952c-3662407dde00
Product NDC
49884-882
Form
KIT
Composition / generic term
Lamotrigine
Labeler
Par Health USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20151127
Source listing expiry
20271231

Source-listed ingredients

Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 PACKAGE, COMBINATION (49884-882-99) / 1 KIT in 1 BLISTER PACK · 49884-882-99

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.

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