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Lamotrigine Extended Release
Lamotrigine Extended Release - 49884-564-01 - (lamotrigine extended release)
Drug Information of Lamotrigine Extended Release
| Product NDC: | 49884-564 |
| Proprietary Name: | Lamotrigine Extended Release |
| Non Proprietary Name: | lamotrigine extended release |
| Active Ingredient(s): | 200 mg/1 & nbsp; lamotrigine extended release |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lamotrigine Extended Release
| Product NDC: | 49884-564 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201791 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130118 |
Package Information of Lamotrigine Extended Release
| Package NDC: | 49884-564-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (49884-564-01) |
NDC Information of Lamotrigine Extended Release
| NDC Code | 49884-564-01 |
| Proprietary Name | Lamotrigine Extended Release |
| Package Description | 100 TABLET in 1 BOTTLE (49884-564-01) |
| Product NDC | 49884-564 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lamotrigine extended release |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130118 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | LAMOTRIGINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
