71335-2123 : Ezetimibe 10 mg Oral Tablet


NDC: 71335-2123
Labeler: Bryant Ranch Prepack
Product Type: Human Prescription Drug
Drug Name:  Ezetimibe
Dosage Form: Oral Tablet
Application #: ANDA209838
Rev. Date: 


NDC Package Codes:

  • 71335-2123-1: 30 TABLET IN 1 BOTTLE (71335‑2123‑1)
  • 71335-2123-2: 90 TABLET IN 1 BOTTLE (71335‑2123‑2)
  • 71335-2123-3: 28 TABLET IN 1 BOTTLE (71335‑2123‑3)
  • 71335-2123-4: 18 TABLET IN 1 BOTTLE (71335‑2123‑4)
  • 71335-2123-5: 60 TABLET IN 1 BOTTLE (71335‑2123‑5)

Active Ingredients:

  • Ezetimibe

Dosage Strength:

  • 10 mg

Pharmaceutical Classes:

  • Decreased Cholesterol Absorption [PE]
  • Dietary Cholesterol Absorption Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
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  • 63629-7413 Ezetimibe 10 mg Oral Tablet by Bryant Ranch Prepack
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  • 16714-813 Ezetimibe 10 mg Oral Tablet by Northstar Rx LLC
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  • 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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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.