Product NDC: | 21695-130 |
Proprietary Name: | Topamax |
Non Proprietary Name: | topiramate |
Active Ingredient(s): | 100 mg/1 & nbsp; topiramate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-130 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020505 |
Marketing Category: | NDA |
Start Marketing Date: | 19970101 |
Package NDC: | 21695-130-15 |
Package Description: | 15 TABLET, COATED in 1 BOTTLE (21695-130-15) |
NDC Code | 21695-130-15 |
Proprietary Name | Topamax |
Package Description | 15 TABLET, COATED in 1 BOTTLE (21695-130-15) |
Product NDC | 21695-130 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | topiramate |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 19970101 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | TOPIRAMATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |