NDC 59088-114

PureFe Plus

Ferrous Fumarate

PureFe Plus is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is Ferrous Fumarate; Thiamine Mononitrate; Riboflavin; Niacinamide; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Calcium Pantothenate; Sodium Ascorbate; Magnesium Sulfate, Unspecified; Zinc Sulfate; Cupric Sulfate; Manganese Sulfate.

• Product ID: 59088-114_d726c3d0-9d1f-43ea-8971-30ecba0e87b7
• NDC: 59088-114
• Product Type: Human Prescription Drug
• Proprietary Name: PureFe Plus
• Generic Name: Ferrous Fumarate
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2011-06-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: PureTek Corporation
• Substance Name: FERROUS FUMARATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; MAGNESIUM SULFATE, UNSPECIFIED; ZINC SULFATE; CUPRIC SULFATE; MANGANESE SULFATE
• Active Ingredient Strength: 106 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
• Pharm Classes: Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 59088-114-59

100 CAPSULE in 1 BOTTLE, PLASTIC (59088-114-59)

• Marketing Start Date: 2011-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59088-114-59 [59088011459]

PureFe Plus CAPSULE

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2011-06-01
• Marketing End Date: 2019-05-28

Drug Details

Active Ingredients

Ingredient	Strength
FERROUS FUMARATE	106 mg/1

OpenFDA Data

• SPL SET ID: 578a7991-b26a-4544-9836-d5018eaeff37
• Manufacturer:
  • PureTek Corporation
• UNII:
  • 25X51I8RD4
  • 68Y4CF58BV
  • W00LYS4T26
  • 568ET80C3D
  • DE08037SAB
  • LRX7AJ16DT
  • R5L488RY0Q
  • TLM2976OFR
  • 89DS0H96TB
  • 8K0I04919X
  • 935E97BOY8
  • S033EH8359
  • P6YC3EG204
• RxNorm Concept Unique ID - RxCUI:
  • 1314654
• UPC Code:
  • 0731477211773

Pharmacological Class

• Nicotinic Acid [EPC]
• Nicotinic Acids [CS]
• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]
• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Copper [CS]
• Copper-containing Intrauterine Device [EPC]
• Decreased Embryonic Implantation [PE]
• Decreased Sperm Motility [PE]
• Inhibit Ovum Fertilization [PE]