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Halothane

Generic Name
Halothane
Drug Type
Small Molecule
Chemical Formula
C2HBrClF3
CAS Number
151-67-7
Unique Ingredient Identifier
UQT9G45D1P

Overview

A nonflammable, halogenated, hydrocarbon anesthetic that provides relatively rapid induction with little or no excitement. Analgesia may not be adequate. nitrous oxide is often given concomitantly. Because halothane may not produce sufficient muscle relaxation, supplemental neuromuscular blocking agents may be required. (From AMA Drug Evaluations Annual, 1994, p178)

Indication

For the induction and maintenance of general anesthesia

Associated Conditions

  • Anesthesia therapy

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2008/12/29
Not Applicable
Completed
Nanjing Medical University

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

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
HALOTHANE
bimeda-mtc animal health inc
00346314
Solution - Inhalation
99.99 %
12/31/1975
FLUOTHANE ANESTHETIC
ayerst laboratories
00052825
Liquid - Inhalation
null NIL / NIL
12/31/1958
HALOTHANE LIQ 99.9%
halocarbon laboratories, a division of halocarbon products corp
00589187
Liquid - Inhalation
99.9 %
12/31/1971
FLUOTHANE LIQ INH 1000MG/GM
wyeth-ayerst canada inc.
02042150
Liquid - Inhalation
1 G / G
12/31/1994

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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