0378-5186 : Prasugrel 10 mg Oral Tablet, Film Coated
NDC: | 0378-5186 |
Labeler: | Mylan Pharmaceuticals Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Prasugrel |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA205927 |
Rev. Date: |
Appearance:
Markings: | M;PH2 |
Shapes: |
Oval |
Colors: |
Brown |
Size (mm): | 11 |
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:
- 0378-5186-93: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (0378‑5186‑93)
Active Ingredients:
- Prasugrel Hydrochloride
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Ferrosoferric Oxide
- Crospovidone (15 Mpa.s At 5%)
- Glyceryl Dibehenate
- Hypromellose, Unspecified
- Lactose Monohydrate
- Mannitol
- Starch, Corn
- Ferric Oxide Red
- Sucrose, 6-stearate
- Titanium Dioxide
- Triacetin
- Ferric Oxide Yellow
Pharmaceutical Classes:
- Decreased Platelet Aggregation [PE]
- P2Y12 Platelet Inhibitor [EPC]
- P2Y12 Receptor Antagonists [MoA]
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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.