Lamotrigine
- Product NDC
- 60760-474
- 11-digit product format
- 607600474
- Labeler code
- 60760
- Product ID
- 60760-474_c2518126-b70d-896f-e053-2a95a90a70ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077633
- Marketing category
- ANDA
- Marketing start
- 2021-04-29
- Marketing end
- 0000-00-00
- Substance
- LAMOTRIGINE
- Active strength
- 25 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-474-30 | 60760047430 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-474-30) | 30 tablet | 2021-04-29 | 0000-00-00 | No | No | Current |