NDC 58809-725

Active FE

.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Dl-, Thiamine Hydrochloride, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Iron Pentacarbonyl, Magnesium Oxide, Zinc Oxide, And Cupric Oxide

Active FE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Gm Pharmaceuticals, Inc.. The primary component is .beta.-carotene; Ascorbic Acid; Cholecalciferol; .alpha.-tocopherol Acetate, Dl-; Thiamine Hydrochloride; Riboflavin; Niacinamide; Pyridoxine Hydrochloride; Folic Acid; Cyanocobalamin; Iron Pentacarbonyl; Magnesium Oxide; Zinc Oxide; Cupric Oxide.

• Product ID: 58809-725_8fd68a8d-c88f-4f08-b24c-9eac6e622851
• NDC: 58809-725
• Product Type: Human Prescription Drug
• Proprietary Name: Active FE
• Generic Name: .beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Dl-, Thiamine Hydrochloride, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Iron Pentacarbonyl, Magnesium Oxide, Zinc Oxide, And Cupric Oxide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2013-11-11
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: GM Pharmaceuticals, Inc.
• Substance Name: .BETA.-CAROTENE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, DL-; THIAMINE HYDROCHLORIDE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; IRON PENTACARBONYL; MAGNESIUM OXIDE; ZINC OXIDE; CUPRIC OXIDE
• Active Ingredient Strength: 2100 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1
• Pharm Classes: Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 58809-725-30

1 BOTTLE in 1 CARTON (58809-725-30) > 30 TABLET in 1 BOTTLE

• Marketing Start Date: 2013-11-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58809-725-30 [58809072530]

Active FE TABLET

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2013-11-11
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
.BETA.-CAROTENE	2100 [iU]/1

OpenFDA Data

• SPL SET ID: bf9624d8-b2ef-45a4-9ad6-a3b8701e76b7
• Manufacturer:
  • GM Pharmaceuticals, Inc.
• UNII:
  • 25X51I8RD4
  • 3A3U0GI71G
  • M572600E5P
  • WR1WPI7EW8
  • PQ6CK8PD0R
  • 1C6V77QF41
  • V1XJQ704R4
  • 68Y4CF58BV
  • TLM2976OFR
  • SOI2LOH54Z
  • 01YAE03M7J
  • 935E97BOY8
  • 6WQ62TAQ6Z
  • P6YC3EG204
• UPC Code:
  • 0358809725304

Pharmacological Class

• Vitamin C [EPC]
• Ascorbic Acid [CS]
• Vitamin D [CS]
• Vitamin D [EPC]
• Vitamin B6 Analog [EPC]
• Vitamin B 6 [Chemical/Ingredient]
• Analogs/Derivatives [Chemical/Ingredient]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]
• Calculi Dissolution Agent [EPC]
• Magnesium Ion Exchange Activity [MoA]
• Osmotic Laxative [EPC]
• Osmotic Activity [MoA]
• Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
• Increased Large Intestinal Motility [PE]
• Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]

Medicade Reported Pricing

58809072530 ACTIVE FE TABLET

Pricing Unit: EA | Drug Type: