NDC 62756-200-18
TIAGABINE HYDROCHLORIDE 2 mg/1
TIAGABINE HYDROCHLORIDE · TABLET, FILM COATED
TIAGABINE HYDROCHLORIDE is a tablet, film coated containing tiagabine hydrochloride at a strength of 2 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- TIAGABINE HYDROCHLORIDE
- Generic Name
- TIAGABINE HYDROCHLORIDE
- NDC Code (Package)
62756-200-18- NDC Code (Product)
62756-200- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 2 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA077555
- Marketing Start
- 11/04/2011
Recall History
No Recall HistoryView Full Drug Page
TIAGABINE HYDROCHLORIDE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.