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LAMOTRIGINE
LAMOTRIGINE - 16590-802-30 - (LAMOTRIGINE)
Drug Information of LAMOTRIGINE
| Product NDC: | 16590-802 |
| Proprietary Name: | LAMOTRIGINE |
| Non Proprietary Name: | LAMOTRIGINE |
| Active Ingredient(s): | 100 mg/1 & nbsp; LAMOTRIGINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LAMOTRIGINE
| Product NDC: | 16590-802 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076388 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101207 |
Package Information of LAMOTRIGINE
| Package NDC: | 16590-802-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (16590-802-30) |
NDC Information of LAMOTRIGINE
| NDC Code | 16590-802-30 |
| Proprietary Name | LAMOTRIGINE |
| Package Description | 30 TABLET in 1 BOTTLE (16590-802-30) |
| Product NDC | 16590-802 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LAMOTRIGINE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101207 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | LAMOTRIGINE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
