NDC 59088-178 – Pretrate

Magnesium Oxide 200 mg/1; Manganese Sulfate 2.6 mg/1; Vitamin A Acetate 1500 ug/1; Ascorbic Acid 120 mg/1; Cholecalciferol 20 ug/1; .alpha.-tocopherol Acetate,… · Tablet · Oral

Human Prescription Drug

Product NDC59088-178

Product details

Brand name
Pretrate
Generic name
Ferrous Fumarate, Folic Acid
Labeler
PureTek Corporation
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
February 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Blood Coagulation Factor; Calculi Dissolution Agent; Copper Absorption Inhibitor; Osmotic Laxative; Paramagnetic Contrast Agent; Phosphate Binder; Vitamin A; Vitamin B12; Vitamin B6 Analog; Vitamin C; Vitamin D

Active ingredients

Uses, dosage, side effects and warnings for Pretrate →

Package NDC codes (1)

Package NDCDescriptionSince
59088-178-5430 TABLET in 1 BOTTLE, PLASTIC (59088-178-54)Feb 1, 2021