Drug
Who makes tiagabine hydrochloride?
3 companies list tiagabine hydrochloride as a human prescription drug. Forms: tablet; tablet, film coated. Routes: oral.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing tiagabine hydrochloride
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Teva Pharmaceutical Industries Ltd.Canada | tablet, film coated | NDA AUTHORIZED GENERICNDA020646 | 4 | 6 |
| Novadoz Pharmaceuticals LLC | tablet | ANDAANDA214816 | 4 | 0 |
| Sun Pharmaceutical Industries LimitedIndia | tablet, film coated | ANDAANDA077555 | 2 | 13 |
Bulk ingredient listings
- MAHI DRUGS PRIVATE LIMITEDIndia · 1 NDC
- MSN Life Sciences Private LimitedIndia · 1 NDC
Enquiry
Common questions
- Who makes tiagabine hydrochloride?
- 3 companies list tiagabine hydrochloride as a human prescription drug in the openFDA NDC Directory, led by Teva Pharmaceutical Industries Ltd., Novadoz Pharmaceuticals LLC, Sun Pharmaceutical Industries Limited. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic tiagabine hydrochloride?
- 2 companies list tiagabine hydrochloride under an abbreviated new drug application (ANDA), the application type used for generics. Listing status is from the NDC Directory; it is not a statement of availability.
- Who supplies tiagabine hydrochloride active ingredient?
- 2 companies list tiagabine hydrochloride as a bulk ingredient, including MAHI DRUGS PRIVATE LIMITED, MSN Life Sciences Private Limited.