0245-0036 : Prevalite 4 g/5.5g Oral Powder, for Suspension


NDC: 0245-0036
Labeler: Upsher-smith Laboratories Inc.
Product Type: Human Prescription Drug
Drug Name:  Prevalite
Dosage Form: Oral Powder, for Suspension
Application #: ANDA073263
Rev. Date: 


NDC Package Codes:

  • 0245-0036-23: 231 G IN 1 CAN (0245‑0036‑23)
  • 0245-0036-42: 42 PACKET IN 1 CARTON (0245‑0036‑42) > 5.5 G IN 1 PACKET (0245‑0036‑89)
  • 0245-0036-60: 60 PACKET IN 1 CARTON (0245‑0036‑60) > 5.5 G IN 1 PACKET (0245‑0036‑89)

Active Ingredients:

  • Cholestyramine

Dosage Strength:

  • 4 g/5.5g

Pharmaceutical Classes:

  • Bile Acid Sequestrant [EPC]
  • Bile-acid Binding Activity [MoA]

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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.