| NDC Code | 0173-0781-00 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0781-00) |
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| Product NDC | 0173-0781 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lamictal |
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| Proprietary Name Suffix | Xr |
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| Non-Proprietary Name | Lamotrigine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20110815 |
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| Marketing Category Name | NDA |
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| Application Number | NDA022115 |
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| Manufacturer | GlaxoSmithKline LLC |
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| Substance Name | LAMOTRIGINE |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA] |
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