10122-902 : 12 Hr Zyflo 600 mg Extended Release Tablet
NDC: | 10122-902 |
Labeler: | Cornerstone Therapeutics Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Zyflo CR |
Dosage Form: | Oral Tablet, Multilayer, Extended Release |
Application #: | NDA022052 |
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. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 10122-902-12: 120 TABLET, MULTILAYER, EXTENDED RELEASE IN 1 BOTTLE (10122‑902‑12)
- 10122-902-20: 20 TABLET, MULTILAYER, EXTENDED RELEASE IN 1 BOTTLE (10122‑902‑20)
Active Ingredients:
- Zileuton
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Starch, Corn
- Sodium Starch Glycolate Type a Potato
Pharmaceutical Classes:
- 5-Lipoxygenase Inhibitors [MoA]
- Decreased Leukotriene Production [PE]
- 5-Lipoxygenase Inhibitor [EPC]
NDC QR Code
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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.