Prescription Drug Information: MagneBind 400 Rx

MAGNEBIND 400 RX- magnesium carbonate, calcium carbonate and folic acid tablet, film coated
Nephro-Tech, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Description

MagneBind 400 Rx is a prescription folic acid supplement with additional nutrients for kidney diaylsis patients. MagneBind 400 Rx is a pink, film-coated, oval shaped tablet.

Suggested Dosage

1-3 tablets with each meal as directed by the physician.

Contraindications

Patients who are hypermagnesemic or who have impaired renal function and are not being dialyzed should not be prescribed MagneBind 400 Rx.

Package Label/Principal Display Panel

59528-0416-05

Rx Only

MagneBind 400 Rx

Mineral/Vitamin Supplement

150 tablets

MagneBind 400 Rx label
(click image for full-size original)
MAGNEBIND 400 RX
vitamin/mineral supplement with magnesium carbonate, calcium carbonate and folic acid tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59528-0416
Route of Administration oral DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MAGNESIUM CARBONATE (CARBONATE ION) MAGNESIUM CARBONATE 115 mg
CALCIUM CARBONATE (CARBONATE ION) CALCIUM CARBONATE 80 mg
FOLIC ACID (FOLIC ACID) FOLIC ACID 1 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
HYDROXYPROPYL CELLULOSE
POLYVINYL ALCOHOL
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL 200
TITANIUM DIOXIDE
TALC
SILICON DIOXIDE
FD&C RED NO. 40
Product Characteristics
Color pink Score no score
Shape OVAL Size 16mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59528-0416-5 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 10/18/1999
Labeler — Nephro-Tech, Inc. (878520485)
Registrant — Nephro-Tech, Inc. (878520485)
Establishment
Name Address ID/FEI Operations
Vitamer/VitaCeutical Labs 806784679 manufacture (59528-0416)

Revised: 02/2014 Nephro-Tech, Inc.

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