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
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/04/12 | Phase 2 | Not yet recruiting | Sahlgrenska University Hospital, Sweden | ||
2021/01/07 | Not Applicable | Completed | Aalborg University | ||
2020/12/21 | Not Applicable | Completed | |||
2020/10/19 | Not Applicable | Completed | Aalborg University | ||
2020/09/18 | Not Applicable | Completed | Aalborg University | ||
2019/10/04 | Not Applicable | Completed | Aalborg University | ||
2019/08/15 | Not Applicable | Completed | |||
2016/09/05 | Phase 1 | Completed | |||
2013/10/16 | Not Applicable | Completed | Guangzhou Institute of Respiratory Disease | ||
2012/11/01 | Phase 1 | Completed | Anergis |
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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