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TIAGABINE HYDROCHLORIDE
TIAGABINE HYDROCHLORIDE - 62756-200-83 - (TIAGABINE HYDROCHLORIDE)
Drug Information of TIAGABINE HYDROCHLORIDE
| Product NDC: | 62756-200 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TIAGABINE HYDROCHLORIDE
| Product NDC: | 62756-200 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077555 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111104 |
Package Information of TIAGABINE HYDROCHLORIDE
| Package NDC: | 62756-200-83 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (62756-200-83) |
NDC Information of TIAGABINE HYDROCHLORIDE
| NDC Code | 62756-200-83 |
| Proprietary Name | TIAGABINE HYDROCHLORIDE |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (62756-200-83) |
| Product NDC | 62756-200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TIAGABINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111104 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| 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] |
