68462-311 : Teriflunomide 7 mg Oral Tablet, Film Coated
NDC: | 68462-311 |
Labeler: | Glenmark Pharmaceuticals Inc., USA |
Product Type: | Human Prescription Drug |
Drug Name: | Teriflunomide |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA209663 |
Rev. Date: |
Appearance:
Markings: | G;43 |
Shapes: |
Round |
Colors: |
Green |
Size (mm): | 6 |
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:
- 68462-311-84: 2 BLISTER PACK IN 1 CARTON (68462‑311‑84) > 14 TABLET, FILM COATED IN 1 BLISTER PACK
- 68462-311-85: 1 BLISTER PACK IN 1 CARTON (68462‑311‑85) > 5 TABLET, FILM COATED IN 1 BLISTER PACK
Active Ingredients:
- Teriflunomide
Dosage Strength:
- 7 mg
Inactive Ingredients:
- Starch, Corn
- Silicon Dioxide
- Hydroxypropyl Cellulose, Unspecified
- Lactose Monohydrate
- Magnesium Stearate
- Microcrystalline Cellulose
- Sodium Starch Glycolate Type a Potato
- Hypromellose, Unspecified
- Polyethylene Glycol 400
- Talc
- Titanium Dioxide
- Fd&c Blue No. 2
- Ferric Oxide Yellow /
Pharmaceutical Classes:
- Pyrimidine Synthesis Inhibitor [EPC]
- Dihydroorotate Dehydrogenase Inhibitors [MoA]
Related Products:
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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.