0093-8076 : Tiagabine Hydrochloride 16 mg Oral Tablet, Film Coated
NDC: | 0093-8076 |
Labeler: | Teva Pharmaceuticals USA, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Tiagabine Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | NDA020646 |
Rev. Date: |
Appearance:
Markings: | C;416 |
Shapes: |
Oval |
Colors: |
Blue |
Size (mm): | 13 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 0093-8076-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑8076‑56)
Active Ingredients:
- Tiagabine Hydrochloride
Dosage Strength:
- 16 mg
Inactive Ingredients:
- Ascorbic Acid
- Silicon Dioxide
- Crospovidone, Unspecified
- Hydrogenated Soybean Oil
- Hydroxypropyl Cellulose, Unspecified
- Hypromellose, Unspecified
- Anhydrous Lactose
- Magnesium Stearate
- Microcrystalline Cellulose
- Starch, Corn
- Stearic Acid
- Titanium Dioxide
- Fd&c Blue No. 2 /
Pharmaceutical Classes:
- Anti-epileptic Agent [EPC]
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
Related Products:
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- 69189-0602 Tiagabine Hydrochloride 4 mg Oral Tablet, Film Coated by Avera Mckennan Hospital
- 69238-1104 Tiagabine Hydrochloride 2 mg Oral Tablet by Amneal Pharmaceuticals LLC
- 69238-1105 Tiagabine Hydrochloride 4 mg Oral Tablet by Amneal Pharmaceuticals LLC
- 69238-1106 Tiagabine Hydrochloride 12 mg Oral Tablet by Amneal Pharmaceuticals LLC
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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.