Pharmaceutical particulars : מידע רוקחי

6. PHARMACEUTICAL PARTICULARS
6.1 List of excipients

Sodium chloride,
Sodium metabisulfite (E223),
Tartaric acid,
Water for injection.

6.2 Incompatibilities
Adrenaline may be inactivated in alkaline solutions or in the presence of oxidising agents such as sodium bicarbonate, halogens, permanganates, chromates, nitrates, nitrites and salts of 
easily reducible metals such as iron, copper and zinc. If adrenaline and sodium bicarbonate need to be administered, they should be injected separately.

6.3 Shelf life

The expiry date of the product is indicated on the packaging materials.
Shelf life after dilution
The product should be used immediately after dilution.
Shelf life after first opening of the pack
The product should be administered immediately after opening.
6.4 Special precautions for storage

Store in the original package below 25ºC. Protect from light.

6.5 Nature and contents of container
Brown glass ampoules.
Each pack contains 10 ampoules of 1 ml.

6.6 Special precautions for disposal and other handling

Single-use containers. Discard any unused contents remaining after administration.
This medicinal product should only be used if the container is undamaged and the solution is clear.

Any unused medicinal product and all materials that have come into contact with it should be disposed of in accordance with local requirements.


7. LICENCE HOLDER AND MANUFACTURER
Teva Pharmaceutical Industries Ltd.,
P.O.Box 3190, Petah Tikva 49131, Israel