TIAGABINE HYDROCHLORIDE 2 mg/1
TIAGABINE HYDROCHLORIDE · TABLET, FILM COATED · Sun Pharmaceutical Industries, Inc.
TIAGABINE HYDROCHLORIDE is a tablet, film coated containing tiagabine hydrochloride at 2 mg/1, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- TIAGABINE HYDROCHLORIDE
- Generic Name
- TIAGABINE HYDROCHLORIDE
- 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 HistoryFrequently Asked Questions
What is TIAGABINE HYDROCHLORIDE used for?
TIAGABINE HYDROCHLORIDE contains TIAGABINE HYDROCHLORIDE. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is TIAGABINE HYDROCHLORIDE a controlled substance?
TIAGABINE HYDROCHLORIDE is not classified as a controlled substance by the DEA.
What is the generic name for TIAGABINE HYDROCHLORIDE?
The generic name for TIAGABINE HYDROCHLORIDE is TIAGABINE HYDROCHLORIDE. There are 8 other brand versions of TIAGABINE HYDROCHLORIDE.
What is the NDC code for TIAGABINE HYDROCHLORIDE 2 mg/1?
The NDC (National Drug Code) for TIAGABINE HYDROCHLORIDE 2 mg/1 is 62756-200, listed by Sun Pharmaceutical Industries, Inc..
Other TIAGABINE HYDROCHLORIDE Dosages
Other Tiagabine Brands
See all →- Tiagabine Hydrochloride2 mg/172205-084
- Tiagabine Hydrochloride4 mg/10093-5031
- Tiagabine Hydrochloride4 mg/172205-085
- Tiagabine Hydrochloride12 mg/172205-086
- Tiagabine Hydrochloride16 mg/172205-087
- Tiagabine Hydrochloride2 mg/10093-5030
- Tiagabine Hydrochloride12 mg/10093-8072
- Tiagabine Hydrochloride16 mg/10093-8076
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)