NDC 0517-6410

Manganese Sulfate

Manganese Sulfate

Manganese Sulfate is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by American Regent, Inc.. The primary component is Manganese Sulfate.

• Product ID: 0517-6410_4022027e-31f8-452c-8f4a-b8d47b37e86d
• NDC: 0517-6410
• Product Type: Human Prescription Drug
• Proprietary Name: Manganese Sulfate
• Generic Name: Manganese Sulfate
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 1990-09-30
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: American Regent, Inc.
• Substance Name: MANGANESE SULFATE
• Active Ingredient Strength: 0 mg/mL
• Pharm Classes: Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0517-6410-25

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6410-25) > 10 mL in 1 VIAL, SINGLE-DOSE

• Marketing Start Date: 1990-09-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0517-6410-25 [00517641025]

Manganese Sulfate INJECTION, SOLUTION

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1990-09-30

Drug Details

Active Ingredients

Ingredient	Strength
MANGANESE SULFATE	.1 mg/mL

OpenFDA Data

• SPL SET ID: 9298b254-4311-46cd-9244-8651dd87417e
• Manufacturer:
  • American Regent, Inc.
• UNII:
  • W00LYS4T26
• RxNorm Concept Unique ID - RxCUI:
  • 237522
• UPC Code:
  • 0305176410258

Pharmacological Class

• Magnetic Resonance Contrast Activity [MoA]
• Paramagnetic Contrast Agent [EPC]