NDC 13668-049 – Lamotrigine

Lamotrigine 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC13668-049

Product details

Brand name
Lamotrigine
Generic name
Lamotrigine
Labeler
Torrent Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078947
Marketed since
January 27, 2009
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lamotrigine →

Package NDC codes (6)

Package NDCDescriptionSince
13668-049-01100 TABLET in 1 BOTTLE (13668-049-01)Jan 27, 2009
13668-049-05500 TABLET in 1 BOTTLE (13668-049-05)Jan 27, 2009
13668-049-131300 TABLET in 1 BOTTLE (13668-049-13)Jan 27, 2009
13668-049-3030 TABLET in 1 BOTTLE (13668-049-30)Jan 27, 2009
13668-049-6060 TABLET in 1 BOTTLE (13668-049-60)Jan 27, 2009
13668-049-6490 TABLET in 1 DOSE PACK (13668-049-64)Jan 27, 2009

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