71770-100 : Siklos 100 mg Oral Tablet, Film Coated
| NDC: | 71770-100 |
| Labeler: | Medunik |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Siklos |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA208843 |
| Rev. Date: |
Appearance:
| Markings: | 100 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 6 |
| 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:
- 71770-100-10: 174 G IN 1 BOTTLE (71770‑100‑10)
- 71770-100-60: 1 BOTTLE IN 1 CARTON (71770‑100‑60) > 60 TABLET, FILM COATED IN 1 BOTTLE
Active Ingredients:
- Hydroxyurea
Dosage Strength:
- 100 mg
Inactive Ingredients:
- Microcrystalline Cellulose
- Silicon Dioxide
- Sodium Stearyl Fumarate
- Dimethylaminoethyl Methacrylate - Butyl Methacrylate - Methyl Methacrylate Copolymer
- Isopropyl Alcohol /
Pharmaceutical Classes:
- Antimetabolite [EPC]
- Urea [CS]
Related Products:
Based on records with the same trade name.- 71770-105 Siklos 100 mg Oral Tablet, Film Coated by Medunik
- 71770-120 Siklos 1000 mg Oral Tablet, Film Coated by Medunik
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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.