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Topiramate
Topiramate - 49349-820-02 - (Topiramate)
Drug Information of Topiramate
| Product NDC: | 49349-820 |
| Proprietary Name: | Topiramate |
| Non Proprietary Name: | Topiramate |
| Active Ingredient(s): | 200 mg/1 & nbsp; Topiramate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Topiramate
| Product NDC: | 49349-820 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090278 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111117 |
Package Information of Topiramate
| Package NDC: | 49349-820-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-820-02) |
NDC Information of Topiramate
| NDC Code | 49349-820-02 |
| Proprietary Name | Topiramate |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-820-02) |
| Product NDC | 49349-820 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Topiramate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111117 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | TOPIRAMATE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
