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tiagabine hydrochloride
tiagabine hydrochloride - 55253-600-30 - (tiagabine hydrochloride)
Drug Information of tiagabine hydrochloride
| Product NDC: | 55253-600 |
| Proprietary Name: | tiagabine hydrochloride |
| Non Proprietary Name: | tiagabine hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; tiagabine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of tiagabine hydrochloride
| Product NDC: | 55253-600 |
| Labeler Name: | CIMA Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020646 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20121226 |
Package Information of tiagabine hydrochloride
| Package NDC: | 55253-600-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (55253-600-30) |
NDC Information of tiagabine hydrochloride
| NDC Code | 55253-600-30 |
| Proprietary Name | tiagabine hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (55253-600-30) |
| Product NDC | 55253-600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tiagabine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121226 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | CIMA Laboratories, Inc. |
| Substance Name | TIAGABINE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
