49884-228 : Ezetimibe 10 mg Oral Tablet
NDC: | 49884-228 |
Labeler: | Par Pharmaceutical Inc |
Product Type: | Human Prescription Drug |
Drug Name: | Ezetimibe |
Dosage Form: | Oral Tablet |
Application #: | ANDA078560 |
Rev. Date: |
Appearance:
Markings: | G80 |
Shapes: |
Capsule |
Colors: |
White |
Size (mm): | 8 |
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:
- 49884-228-05: 500 TABLET IN 1 BOTTLE (49884‑228‑05)
- 49884-228-09: 90 TABLET IN 1 BOTTLE (49884‑228‑09)
- 49884-228-11: 30 TABLET IN 1 BOTTLE (49884‑228‑11)
Active Ingredients:
- Ezetimibe
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Lactose Monohydrate
- Magnesium Stearate
- Povidones
- Sodium Lauryl Sulfate
Pharmaceutical Classes:
- Decreased Cholesterol Absorption [PE]
- Dietary Cholesterol Absorption Inhibitor [EPC]
Related Products:
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- 33342-373 Ezetimibe 10 mg Oral Tablet by Macleods Pharmaceuticals Limited
- 42291-314 Ezetimibe 10 mg Oral Tablet by Avkare, Inc.
- 50090-2717 Ezetimibe 10 mg Oral Tablet by A-s Medication Solutions
- 50090-3087 Ezetimibe 10 mg Oral Tablet by A-s Medication Solutions
- 50090-3402 Ezetimibe 10 mg Oral Tablet by A-s Medication Solutions
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- 50228-379 Ezetimibe 10 mg Oral Tablet by Sciegen Pharmaceuticals Inc
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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.