Tiagabine Hydrochloride - NDC Database
0093-5030 Jun 03, 2016
Tiagabine Hydrochloride 2 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
Tiagabine Hydrochloride 2 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
0093-5031 Jul 18, 2016
Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
69189-0602 Mar 10, 2015
Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Avera Mckennan Hospital
Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Avera Mckennan Hospital
0093-8072 Mar 09, 2018
Tiagabine Hydrochloride 12 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
Tiagabine Hydrochloride 12 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
0093-8076 Mar 09, 2018
Tiagabine Hydrochloride 16 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
Tiagabine Hydrochloride 16 mg Oral Tablet, Film Coated by Teva Pharmaceuticals USA, Inc.
62756-200 Nov 04, 2011
Tiagabine Hydrochloride 2 mg Oral Tablet by Sun Pharmaceutical Industries Limited
Tiagabine Hydrochloride 2 mg Oral Tablet by Sun Pharmaceutical Industries Limited
62756-224 Nov 04, 2011
Tiagabine Hydrochloride 4 mg Oral Tablet by Sun Pharmaceutical Industries Limited
Tiagabine Hydrochloride 4 mg Oral Tablet by Sun Pharmaceutical Industries Limited
Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.