TIAGABINE HYDROCHLORIDE - TIAGABINE HYDROCHLORIDE
Navigation: NDC > Supplier starting with: S > SUN PHARMACEUTICAL INDUSTRIES LIMITED| Field | Value |
|---|---|
| NDC Code: | 62756-200 |
| Proprietary Name: | TIAGABINE HYDROCHLORIDE |
| Suffix: | |
| Non-Proprietary Name: | TIAGABINE HYDROCHLORIDE |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 04-11-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA077555 |
| Labeler: | SUN PHARMACEUTICAL INDUSTRIES LIMITED |
| Substance Name: | TIAGABINE HYDROCHLORIDE |
| Active Numerator Strength: | 2 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
| DEA Schedule: |