NDC 58607-112

Myferon 150 Forte

Iron Sucrose, Folic Acid, Cyanocobalamin

Myferon 150 Forte is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Martin Ekwealor Pharmaceuticals, Inc.. The primary component is Iron Sucrose; Folic Acid; Cyanocobalamin.

• Product ID: 58607-112_24af9e28-be37-44a7-89c9-629f29b621e9
• NDC: 58607-112
• Product Type: Human Prescription Drug
• Proprietary Name: Myferon 150 Forte
• Generic Name: Iron Sucrose, Folic Acid, Cyanocobalamin
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1996-12-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: MARTIN EKWEALOR PHARMACEUTICALS, INC.
• Substance Name: IRON SUCROSE; FOLIC ACID; CYANOCOBALAMIN
• Active Ingredient Strength: 150 mg/1; mg/1; ug/1
• Pharm Classes: Iron [CS],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],Vitamin B 12 [CS],Vitamin B12 [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 58607-112-00

100 BLISTER PACK in 1 BOX (58607-112-00) > 10 CAPSULE in 1 BLISTER PACK

• Marketing Start Date: 1996-12-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58607-112-00 [58607011200]

Myferon 150 Forte CAPSULE

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1996-12-01
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
IRON SUCROSE	150 mg/1

OpenFDA Data

• SPL SET ID: ed2308e3-5310-41bd-9333-615c26183493
• Manufacturer:
  • MARTIN EKWEALOR PHARMACEUTICALS, INC.
• UNII:
  • 935E97BOY8
  • FZ7NYF5N8L
  • P6YC3EG204
• RxNorm Concept Unique ID - RxCUI:
  • 309606

Pharmacological Class

• Iron [CS]
• Parenteral Iron Replacement [EPC]
• Phosphate Binder [EPC]
• Phosphate Chelating Activity [MoA]
• Vitamin B 12 [CS]
• Vitamin B12 [EPC]