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MagneBind 400 RX: Package Insert / Prescribing Info

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 3, 2025.

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.

Related/similar drugs

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)