NDC 72205-087-30
Tiagabine Hydrochloride 16 mg/1
Tiagabine Hydrochloride · TABLET
Tiagabine Hydrochloride is a tablet containing tiagabine hydrochloride at a strength of 16 mg/1. Manufactured by Novadoz Pharmaceuticals LLC.
Key Facts
- Brand Name
- Tiagabine Hydrochloride
- Generic Name
- Tiagabine Hydrochloride
- NDC Code (Package)
72205-087-30- NDC Code (Product)
72205-087- Manufacturer
- Novadoz Pharmaceuticals LLC
- Strength
- 16 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA214816
- Marketing Start
- 11/23/2021
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.