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PureFe Plus - 59088-114-59 - (Ferrous Fumarate)

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Drug Information Labeler Information Package Information NDC Record

Drug Information of PureFe Plus

Product NDC: 59088-114
Proprietary Name: PureFe Plus
Non Proprietary Name: Ferrous Fumarate
Active Ingredient(s): 10; .8; 15; 106; 1; 6.9; 1.3; 30; 5; 6; 200; 10; 18.2    mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp;   Ferrous Fumarate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of PureFe Plus

Product NDC: 59088-114
Labeler Name: PureTek Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110601

Package Information of PureFe Plus

Package NDC: 59088-114-59
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (59088-114-59)

NDC Information of PureFe Plus

NDC Code 59088-114-59
Proprietary Name PureFe Plus
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (59088-114-59)
Product NDC 59088-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ferrous Fumarate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name PureTek Corporation
Substance Name CALCIUM PANTOTHENATE; CUPRIC SULFATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM SULFATE, UNSPECIFIED; MANGANESE SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE
Strength Number 10; .8; 15; 106; 1; 6.9; 1.3; 30; 5; 6; 200; 10; 18.2
Strength Unit mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]

Complete Information of PureFe Plus


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