59088-795 : Folcyteine Oral Tablet


NDC: 59088-795
Labeler: Puretek Corporation
Product Type: Human Prescription Drug
Drug Name: Folcyteine
Dosage Form: Oral Tablet
Rev. Date: 


NDC Package Codes:

  • 59088-795-54: 30 TABLET IN 1 BOTTLE, PLASTIC (59088‑795‑54)

Active Ingredients:

  • Acetylcysteine
  • Calcium Citrate
  • Cholecalciferol
  • Folic Acid
  • Magnesium Citrate

Dosage Strength:

  • 200 mg
  • 47 mg
  • 800 [iU]/1
  • 1000 ug/1
  • 16 mg

Pharmaceutical Classes:

  • Antidote [EPC]
  • Antidote for Acetaminophen Overdose [EPC]
  • Blood Coagulation Factor [EPC]
  • Calcium [CS]
  • Calculi Dissolution Agent [EPC]
  • Cations
  • Divalent [CS]
  • Decreased Respiratory Secretion Viscosity [PE]
  • Increased Coagulation Factor Activity [PE]
  • Increased Glutathione Concentration [PE]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Mucolytic [EPC]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Phosphate Binder [EPC]
  • Phosphate Chelating Activity [MoA]
  • Reduction Activity [MoA]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
  • Vitamin D [CS]
  • Vitamin D [EPC]

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.