59630-551 : Mulpleta 3 mg Oral Tablet, Film Coated
| NDC: | 59630-551 |
| Labeler: | Shionogi Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Mulpleta |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA210923 |
| Rev. Date: |
Appearance:
| Markings: | 551;3 |
| Shapes: |
Round |
| Colors: |
 Red |
| Size (mm): | 7 |
| 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:
- 59630-551-07: 1 DOSE PACK IN 1 CARTON (59630‑551‑07) > 7 TABLET, FILM COATED IN 1 DOSE PACK
- 59630-551-77: 1 DOSE PACK IN 1 CARTON (59630‑551‑77) > 7 TABLET, FILM COATED IN 1 DOSE PACK
Active Ingredients:
- Lusutrombopag
Dosage Strength:
- 3 mg
Inactive Ingredients:
- Mannitol
- Microcrystalline Cellulose
- Magnesium Oxide
- Sodium Lauryl Sulfate
- Hydroxypropyl Cellulose, Unspecified
- Carboxymethylcellulose Calcium
- Magnesium Stearate
- Hypromellose, Unspecified
- Triethyl Citrate
- Titanium Dioxide
- Ferric Oxide Red
- Talc /
NDC QR Code
Scan the QR code below to easily reference this data in the future:
< Prev: 59630-503Next: 59630-574 >
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.