| NDC Code | 52536-251-03 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52536-251-03) |
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| Product NDC | 52536-251 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lamotrigine |
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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 | 20140317 |
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| End Marketing Date | 20180430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202887 |
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| Manufacturer | Wilshire Pharmaceuticals, Inc. |
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| Substance Name | LAMOTRIGINE |
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| Strength | 50 |
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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],Mood Stabilizer [EPC] |
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