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Manganese

Generic Name
Manganese
Brand Names
Concept Ob, Multitrace-4, Multitrace-5, Multrys, Tandem Plus
Drug Type
Small Molecule
Chemical Formula
Mn
CAS Number
7439-96-5
Unique Ingredient Identifier
H6EP7W5457

Overview

Manganese is a transition metal with a molar mass of 54.94g/mol. Manganese is considered critical for human health, and plays important roles in development, metabolism, and the antioxidant system. That said, excessive manganese intake is associated with manganism, a neurodegenerative disorder that causes dopaminergic neuronal death and parkinsonian-like symptoms.

Indication

Indicated for use as a supplement to intravenous solutions given for Total Parenteral Nutrition (TPN). Administration helps to maintain plasma levels and to prevent depletion of endogenous stores and subsequent deficiency symptoms.

Associated Conditions

No associated conditions information available.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Nutritional Specialties, Inc.
83027-0036
ORAL
12 [hp_X] in 1 mL
4/14/2025
Exeltis USA, Inc.
0642-0207
ORAL
1.5 mg in 1 1
1/2/2023
Deseret Biologicals, Inc.
43742-2244
ORAL
12 [hp_X] in 1 mL
5/27/2025
Deseret Biologicals, Inc.
43742-2259
ORAL
16 [hp_X] in 1 mL
4/8/2025
Parasitology Center Inc.
70321-0003
ORAL
15 [hp_X] in 1 mL
5/22/2025
Deseret Biologicals, Inc.
43742-1312
ORAL
8 [hp_X] in 1 mL
5/27/2025
King Bio Inc.
57955-5276
ORAL
10 [hp_X] in 59 mL
5/19/2025
Parasitology Center, Inc.
70321-0002
ORAL
16 [hp_C] in 1 mL
5/22/2025
Dr. Donna Restivo DC
62185-0062
ORAL
8 [hp_X] in 1 mL
5/23/2025
Hospira, Inc.
0409-4091
INTRAVENOUS
0.1 mg in 1 mL
12/6/2023

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
ADDAVEN CONCENTRATE FOR SOLUTION FOR INFUSION
SIN15302P
INFUSION, SOLUTION CONCENTRATE
19.79 mcg/ml
7/24/2017
PEDITRACE CONCENTRATE FOR PARENTERAL INFUSION
SIN08899P
INJECTION
3.6 mcg/ml
9/4/1996

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
CELL-WISE
melaleuca of canada inc.
02236914
Tablet - Oral
1.5 MG / TAB
1/12/1998
DIATHESIS I
bio active canada ltd.
02233598
Liquid - Oral
3 X
5/26/1998
MANGANUM METALLICUM GOUTTE 4CH-30CH
dolisos laboratoires s.a.
00667900
Drops - Oral
3 CH / CH
12/31/1987
APIZELEN
bio active canada ltd.
02233553
Liquid - Oral
12 X
5/26/1998
MANGANUM METALLICUM GRANULE 4CH-30CH
homeocan inc.
01917862
Tablet - Oral
4 CH / TAB
12/31/1991
MANGANUM METALLICUM-INJEEL FORTE LIQ (6D,10D,30D,200D/1.1ML)
02064642
Liquid - Oral
6 D / 1.1 ML
12/31/1994
MANGANUM METALLICUM GRANULE 4CH - 30CH
dolisos laboratoires s.a.
00699535
Tablet - Oral
4 CH / CH
12/31/1987
FORMULA 32460
therapeutic foods co.
00219576
Capsule - Oral
6.3 MG
5/18/1994
TRACE ELEMENTS SOLUTION INJ
david bull laboratories (pty) ltd.
00861979
Solution - Intravenous
1.44 MG / 5 ML
12/31/1991
UNIVERSALTOX
bio active canada ltd.
02233693
Liquid - Oral
3 X
5/26/1998

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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