70756-702 : Alosetron .5 mg Oral Tablet
| NDC: | 70756-702 |
| Labeler: | Lifestar Pharma LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Alosetron |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA213614 |
| Rev. Date: |
Appearance:
| Markings: | LS;702 |
| 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:
- 70756-702-30: 30 TABLET IN 1 BOTTLE (70756‑702‑30)
Active Ingredients:
- Alosetron Hydrochloride
Dosage Strength:
- .5 mg
Inactive Ingredients:
- Lactose Monohydrate
- Cellulose, Microcrystalline
- Starch, Corn
- Magnesium Stearate
- Hypromellose 2910 (6 Mpa.s)
- Polyethylene Glycol 8000
- Titanium Dioxide /
Pharmaceutical Classes:
- Serotonin 3 Receptor Antagonists [MoA]
- Serotonin-3 Receptor Antagonist [EPC]
Related Products:
Based on records with the same trade name.- 70756-701 Alosetron 1 mg Oral Tablet by Lifestar Pharma LLC
- 63629-2517 Alosetron .5 mg Oral Tablet by Bryant Ranch Prepack
- 63629-2518 Alosetron 1 mg Oral Tablet by Bryant Ranch Prepack
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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.