MAGNEBIND 400 RX- vitamin/mineral supplement with magnesium carbonate, calcium carbonate and folic acid tablet, film coated
Carilion Materials Management

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.

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MagneBind 400 Rx magnesium carbonate, calcium carbonate, folic acid tablet, coated

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.

Magnabind 400 rx tabs

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:68151-4243(NDC:59528-0416)
Route of Administration	oral

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D)	MAGNESIUM CARBONATE	115 mg
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	80 mg
FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8)	FOLIC ACID	1 mg

Ingredient Name	Strength
Inactive Ingredients
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
HYDROXYPROPYL CELLULOSE (TYPE H) (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
Color	pink	Score	no score
Shape	OVAL	Size	16mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:68151-4243-5	1 in 1 PACKAGE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		10/18/1999

Labeler - Carilion Materials Management (079239644)

Registrant - Carilion Materials Management (079239644)

Name	Address	ID/FEI	Business Operations
Establishment
Carilion Materials Management		079239644	REPACK(68151-4243)