Tiagabine Hydrochloride 2 mg/1
Tiagabine Hydrochloride · TABLET · Novadoz Pharmaceuticals LLC
Tiagabine Hydrochloride is a tablet containing tiagabine hydrochloride at 2 mg/1, taken oral. Manufactured by Novadoz Pharmaceuticals LLC.
Key Facts
- Brand Name
- Tiagabine Hydrochloride
- Generic Name
- Tiagabine Hydrochloride
- NDC Code (Product)
72205-084- Manufacturer
- Novadoz Pharmaceuticals LLC
- Strength
- 2 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA214816
- Marketing Start
- 11/23/2021
Recall History
SUN PHARMACEUTICAL INDUSTRIES INC
Failed Impurities: Out of Specification (OOS) result observed during Related Substances testing
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is Tiagabine Hydrochloride used for?
Tiagabine Hydrochloride contains Tiagabine Hydrochloride. It is a tablet 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 2 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 72205-084, listed by Novadoz Pharmaceuticals LLC.