MedPath

Ammonia

Generic Name
Ammonia
Brand Names
Kenalog
Drug Type
Small Molecule
CAS Number
7664-41-7

Overview

Ammonia is a naturally-occurring compound with a chemical formula NH3 and structure of trigonal pyramidal geometry. It is a colorless gas with a pungent smell, and become NH4, or ammonium ion, when in water. Although ammonia is used as a food additive in the anhydrous form and serves as a starting material in pharmaceutical and commercial products, it is caustic and hazardous when concentrated. Ammonia gas has been used in the clinical setting as a respiratory stimulant to prevent fainting. The radiolabelled form of ammonia, ammonia N 13, is intravenously administered as a radioactive diagnostic agent for Positron Emission Tomography (PET) imaging of the myocardium to evaluate myocardial perfusion. Ammonia is a natural byproduct of biological and chemical reactions, including decomposition of organic matter, including plants, animals, and animal wastes. It is present in normally present in all tissues constituting a metabolic pool, where it is mostly taken up by glutamic acid and take part in transamination and other reactions, including the synthesis of protein by the Krebs-Hanseleit cycle in the liver . It is proposed that human adults produce about 1000 mmol of ammonia daily, most of which undergoes excretion in the urine.

Indication

No indication information available.

Associated Conditions

  • Skin Irritation
  • Syncope or fainting sensation

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Jiangxi Hemei Pharmaceutical Co., Ltd
84010-128
RESPIRATORY (INHALATION)
15 g in 100 g
5/27/2025
KINKANDO CO., LTD .
51027-0007
TOPICAL
1.1 g in 50 mL
6/10/2025
Washburn Ventures LLC
85764-001
RESPIRATORY (INHALATION)
15 g in 100 g
6/9/2025
Jiangxi Hemei Pharmaceutical Co., Ltd
84010-142
RESPIRATORY (INHALATION)
15 g in 100 g
7/7/2025
Sina Health Inc
70385-2003
RESPIRATORY (INHALATION)
0.045 g in 0.3 mL
2/4/2019
Shenzhen Nanjun Technology Co., Ltd
85590-001
RESPIRATORY (INHALATION)
15 g in 100 g
4/29/2025
Shenzhen Chihai Trading Co., Ltd.
85670-001
TOPICAL
15 g in 100 g
5/7/2025
A-S Medication Solutions
50090-0342
RESPIRATORY (INHALATION)
0.045 g in 0.3 mL
10/12/2020
Platinum Trident Enterprise
85570-1111
NASAL
15 g in 100 g
5/22/2025

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
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
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
BRONCHEX COUGH SYRUP
hilary's distibution ltd.
00756865
Syrup - Oral
2.699 MG / 5 ML
12/31/1988
AMMONIA INHALANTS
trafalgar industries of canada ltd.
00311197
Liquid - Inhalation
13 %
12/31/1964
LINIMENT SOKER
produits francais labs inc.
00166111
Liquid - Topical
.81 ML / 30 G
12/31/1930
AFTER BITE LIQUID 3.61%
tender corporation
00766097
Liquid - Topical
3.61 %
12/31/1990
ESPRIT D'AMMONIAQUE AROMATIQUE
lab valmo enregistré, division of technilab inc.
00766100
Liquid - Nasal ,  Inhalation
1.9 G / 100 ML
12/31/1991
AMMONIA INHALANT
professional disposables international inc.
00485276
Pad - Inhalation
15 %
12/31/1980

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.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.