10122-901 : Zyflo 600 mg Oral Tablet
| NDC: | 10122-901 |
| Labeler: | Cornerstone Therapeutics Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Zyflo |
| Dosage Form: | Oral Tablet |
| Application #: | NDA020471 |
| Rev. Date: |
Appearance:
| Markings: | CT2 |
| Shapes: |
Oval |
| Colors: |
 White |
| 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:
- 10122-901-12: 120 TABLET IN 1 BOTTLE (10122‑901‑12)
Active Ingredients:
- Zileuton
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Crospovidone
- Hydroxypropyl Cellulose (Type H)
- Hypromelloses
- Magnesium Stearate
- Cellulose, Microcrystalline
- Propylene Glycol
- Sodium Starch Glycolate Type a Potato
- Talc
- Titanium Dioxide
- Starch, Corn
Pharmaceutical Classes:
- 5-Lipoxygenase Inhibitor [EPC]
- 5-Lipoxygenase Inhibitors [MoA]
- Decreased Leukotriene Production [PE]
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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.