MedPath

Histamine

Generic Name
Histamine
Brand Names
Activon Arthritis, Ceplene, Rematex
Drug Type
Small Molecule
Chemical Formula
C5H9N3
CAS Number
51-45-6
Unique Ingredient Identifier
820484N8I3

Overview

A depressor amine derived by enzymatic decarboxylation of histidine. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.

Indication

Histamine phosphate is indicated as a diagnostic aid for the evaluation of gastric acid secretory function.

Associated Conditions

  • Migraine

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
King Bio Inc.
57955-9003
ORAL
10 [hp_X] in 59 mL
5/19/2025
Deseret Biologicals, Inc.
43742-2218
ORAL
6 [hp_X] in 1 mL
5/27/2025
Nutritional Specialties, Inc.
83027-0123
ORAL
12 [hp_X] in 1 mL
5/15/2025
Boiron
0220-9303
ORAL
9 [hp_C] in 1 1
5/12/2025
SEVENE USA
76472-5003
SUBLINGUAL
30 [hp_C] in 1 1
5/15/2025
ALK-Abello, Inc.
0268-0247
PERCUTANEOUS
2.75 mg in 1 mL
8/25/2020
Jubilant HollisterStier LLC
65044-9998
PERCUTANEOUS
6 mg in 1 mL
11/1/2023
Home Aide Diagnostics, Inc.
69379-001
TOPICAL
0.035 g in 100 g
7/8/2015
Eight and Company L.L.C
61096-2004
ORAL
200 [hp_C] in 1 mL
5/15/2025
King Bio Inc.
57955-0762
ORAL
12 [hp_X] in 59 mL
5/20/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
10/7/2008

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

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.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
Biochemics Hayfever
120022
Medicine
A
6/22/2005
Allergy Oral Spray
351127
Medicine
A
12/8/2020
Snoreeze Oral Spray
351124
Medicine
A
12/8/2020

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
HISTAMINE PHOSPHATE INJECTION USP LIQ SC
bioniche pharma (canada) ltd
02094673
Liquid - Subcutaneous
1 MG / ML
12/31/1994
HISTATROL
alk-abello inc
00609706
Solution - Intradermal
0.275 MG / ML
12/31/1984
MEDIPLEX 600 - LIQ
mediherb inc.
02116928
Liquid - Oral
14 X / ML
12/19/1996
LUFFEEL NASAL SPRAY
02227738
Spray - Nasal
12 D / 100 ML
3/6/2003
ALLER
botanical laboratories inc.
02233393
Liquid - Oral
12 X
4/15/1998
MIDALGAN
welcker-lyster ltd., division of technilab inc.
00234575
Ointment - Topical
100 MG / 100 G
12/31/1948
HISTAMINUM MURIATICUM
seroyal international inc.
02233758
Globules ,  Tablet ,  Liquid ,  Granules ,  Pellet ,  Drops - Oral
4 X
4/6/1998
ALOPT
terra botanica products ltd.
02233289
Liquid - Oral
30 X
5/25/1998
HISTAMINUM TAB (4CH-30CH)
laboratoires holis inc.
02086697
Tablet - Oral
4 CH / TAB
12/31/1984
HISTAMINE PHOSPHATE INJECTION USP, 1MG/ML
alveda pharmaceuticals inc
02300427
Liquid - Subcutaneous
1 MG / ML
N/A

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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