NDC 59088-008 – Finazol

Vitamin A Acetate 1500 ug/1; Ascorbic Acid 200 mg/1; Cholecalciferol 10 ug/1; .alpha.-tocopherol Acetate, Dl- 45 mg/1; Thiamine Mononitrate 3.25 mg/1;… · Tablet · Oral

Human Prescription Drug

Product NDC59088-008

Product details

Brand name
Finazol
Generic name
Ferrous Fumarate, Folate
Labeler
PureTek Corporation
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
October 11, 2024
Listing expires
December 31, 2026
Pharmacologic class
Blood Coagulation Factor; Calculi Dissolution Agent; Copper Absorption Inhibitor; Folate Analog; Nicotinic Acid; Osmotic Laxative; Osmotic Laxative; Paramagnetic Contrast Agent; Phosphate Binder; Potassium Salt; Vitamin A; Vitamin B6 Analog; Vitamin C; Vitamin D

Active ingredients

Uses, dosage, side effects and warnings for Finazol →

Package NDC codes (1)

Package NDCDescriptionSince
59088-008-5430 TABLET in 1 BOTTLE, PLASTIC (59088-008-54)Oct 11, 2024