59572-730 : Onureg 200 mg Oral Tablet, Film Coated
| NDC: | 59572-730 |
| Labeler: | Celgene Corporation |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Onureg |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA214120 |
| Rev. Date: |
Appearance:
| Markings: | ONU;200 |
| Shapes: |
Oval |
| Colors: |
 Pink |
| Size (mm): | 19 |
| 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:
- 59572-730-07: 7 TABLET, FILM COATED IN 1 BLISTER PACK (59572‑730‑07)
- 59572-730-14: 14 TABLET, FILM COATED IN 1 BOTTLE (59572‑730‑14)
Active Ingredients:
- Azacitidine
Dosage Strength:
- 200 mg
Inactive Ingredients:
- Mannitol
- Microcrystalline Cellulose
- Croscarmellose Sodium
- Magnesium Stearate /
Pharmaceutical Classes:
- Nucleic Acid Synthesis Inhibitors [MoA]
- Nucleoside Metabolic Inhibitor [EPC]
Related Products:
Based on records with the same trade name.- 59572-740 Onureg 300 mg Oral Tablet, Film Coated by Celgene Corporation
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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.