NDC 59088-795 – Folcyteine

Calcium Citrate 47 mg/1; Cholecalciferol 800 [iU]/1; Folic Acid 1000 ug/1; Acetylcysteine 200 mg/1; Magnesium Citrate 16 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59088-795

Product details

Brand name
Folcyteine
Generic name
Multivitamin
Labeler
PureTek Corporation
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
September 14, 2023
Listing expires
December 31, 2027
Pharmacologic class
Antidote; Antidote for Acetaminophen Overdose; Blood Coagulation Factor; Calculi Dissolution Agent; Mucolytic; Osmotic Laxative; Phosphate Binder; Vitamin D

Active ingredients

Uses, dosage, side effects and warnings for Folcyteine →

Package NDC codes (1)

Package NDCDescriptionSince
59088-795-5430 TABLET in 1 BOTTLE, PLASTIC (59088-795-54)Sep 14, 2023