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MagneBind 400 RX Prescribing Information

Package insert / product label
Generic name: magnesium carbonate, calcium carbonate and folic acid tablet
Dosage form: tablet, film coated
Drug class: Vitamin and mineral combinations

Medically reviewed by Drugs.com. Last updated on Mar 11, 2022.

MagneBind 400 RX 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.

MagneBind 400 RX Dosage and Administration

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

MAGNEBIND 400 RX
vitamin/mineral supplement with magnesium carbonate, calcium carbonate and folic acid tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:59528-0416
Route of Administrationoral
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE115 mg
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE80 mg
FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID1 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
POLYVINYL ALCOHOL (UNII: 532B59J990)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TALC (UNII: 7SEV7J4R1U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
FD&C RED NO. 40 (UNII: WZB9127XOA)
Product Characteristics
ColorpinkScoreno score
ShapeOVALSize16mm
FlavorImprint Code
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59528-0416-5150 in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/18/1999
Labeler - Nephro-Tech, Inc. (878520485)
Registrant - Nephro-Tech, Inc. (878520485)
Establishment
NameAddressID/FEIBusiness Operations
Vitamer/VitaCeutical Labs806784679manufacture(59528-0416)