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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Acute Toxicity: oral

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature

Data source

Reference
Reference Type:
secondary source
Title:
APPROVAL PACKAGE FOR: APPLICATION NUMBER 20-825. Pharmacology Review(s).
Bibliographic source:
Food and Drug Administration - Center for Drug Evaluation and research.
Report date:
2000

Materials and methods

Test material

Constituent 1
Chemical structure
Reference substance name:
5-[2-[4-(1,2-benzothiazol-3-yl)piperazin-1-yl]ethyl]-6-chloro-1,3-dihydroindol-2-one;hydrate;hydrochloride
Cas Number:
138982-67-9
Molecular formula:
C21H24Cl2N4O2S
IUPAC Name:
5-[2-[4-(1,2-benzothiazol-3-yl)piperazin-1-yl]ethyl]-6-chloro-1,3-dihydroindol-2-one;hydrate;hydrochloride
Test material form:
solid

Test animals

Species:
mouse
Strain:
not specified
Sex:
male/female

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Doses:
500 and 2000 mg/kg
No. of animals per sex per dose:
3
Control animals:
not specified

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

Sedation was the primary clinical sign. CNS signs tended to have a more rapid onset and prolonged duration with  i. p. dosing (respect p.o. route) . No target organ for toxicity was identified.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
For ziprasidone hydrochloride monohydrate the mouse LD50 is > 2000 mg/kg/bw.
Executive summary:

The acute toxicity of the substance was tested in mice. As a results, the mouse LD50 is > 2000 mg/kg/bw, so the substance is not classified for acute oral toxicity.