Lamotrigine
- Product NDC
- 70518-2093
- 11-digit product format
- 705182093
- Labeler code
- 70518
- Product ID
- 70518-2093_89a7bc7c-e535-4dfe-e053-2995a90a3782
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA079132
- Marketing category
- ANDA
- Marketing start
- 2019-05-21
- Marketing end
- 0000-00-00
- Substance
- LAMOTRIGINE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Anti-epileptic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record