Lamotrigine
- Product NDC
- 50090-4939
- 11-digit product format
- 500904939
- Labeler code
- 50090
- Product ID
- 50090-4939_a03d9536-1fc8-4ae6-8a45-c502df499225
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077633
- Marketing category
- ANDA
- Marketing start
- 2009-01-27
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4939-0 | Lamotrigine | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
| 50090-4939-0 | Lamotrigine | 33 in 1 BOX, UNIT-DOSE | TABLET | 33 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4939 | LAMOTRIGINE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20200319_cde10b44-d1e8-4b0e-821c-1e6bd5b82532.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4939-0 | 50090493900 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-4939-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2020-02-28 | 0000-00-00 | No | No | Current |