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TOPIRAMATE
TOPIRAMATE - 52959-643-30 - (TOPIRAMATE)
Drug Information of TOPIRAMATE
| Product NDC: | 52959-643 |
| Proprietary Name: | TOPIRAMATE |
| Non Proprietary Name: | TOPIRAMATE |
| Active Ingredient(s): | 100 mg/1 & nbsp; TOPIRAMATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TOPIRAMATE
| Product NDC: | 52959-643 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090278 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090327 |
Package Information of TOPIRAMATE
| Package NDC: | 52959-643-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (52959-643-30) |
NDC Information of TOPIRAMATE
| NDC Code | 52959-643-30 |
| Proprietary Name | TOPIRAMATE |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (52959-643-30) |
| Product NDC | 52959-643 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TOPIRAMATE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090327 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | TOPIRAMATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
