Cifran

Country: New Zealand

Language: English

Source: Medsafe (Medicines Safety Authority)

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Active ingredient:

Ciprofloxacin hydrochloride 583.59mg equivalent to ciprofloxacin 500 mg;  

Available from:

Douglas Pharmaceuticals Limited

INN (International Name):

Ciprofloxacin hydrochloride 583.59 mg (equivalent to ciprofloxacin 500 mg)

Dosage:

500 mg

Pharmaceutical form:

Film coated tablet

Composition:

Active: Ciprofloxacin hydrochloride 583.59mg equivalent to ciprofloxacin 500 mg   Excipient: Colloidal silicon dioxide Magnesium stearate Maize starch Microcrystalline cellulose Opadry white OY-S-58910 Purified talc Purified water   Sodium starch glycolate

Units in package:

Blister pack, PVC/PVDC/aluminium foil, 10, 30 tablets, 10

Class:

Prescription

Prescription type:

Prescription

Manufactured by:

Dr Reddy's Laboratories Limited

Product summary:

Package - Contents - Shelf Life: Blister pack, PVC/PVDC/aluminium foil, 10, 30 tablets - 10 - 36 months from date of manufacture stored at or below 25°C

Authorization date:

2002-04-30

Summary of Product characteristics

                                DATA SHEET 
 
 
CIFRAN 
CIPROFLOXACIN HYDROCHLORIDE PH. EUR. 250 MG, 500 MG AND 750 MG FILM
COATED TABLETS 
 
PRESENTATION 
 
Cifran 250 mg tablets: each tablet contains 291.79 mg ciprofloxacin
hydrochloride, equivalent to 250 
mg ciprofloxacin. Tablets are white to off-white, round, film-coated,
embossed with ‘250’ on one side 
and plain on the other side. 
 
Cifran 500 mg tablets: each tablet contains 583.59 mg ciprofloxacin
hydrochloride, equivalent to 500 
mg ciprofloxacin. Tablets are white to off-white, caplet-shaped,
film-coated, embossed with ‘500’ on 
one side and plain on the other side. 
 
Cifran 750 mg tablets: each  tablet contains
875.39 mg ciprofloxacin hydrochloride, equivalent to 750 
mg ciprofloxacin. Tablets are white to off-white, caplet-shaped,
film-coated, embossed with ‘750’ on 
one side and plain on the other side. 
 
USES 
_ACTIONS _
 
Ciprofloxacin is a synthetic broad spectrum antibacterial agent
(ATCCODE: J 01 MA 02). 
Ciprofloxacin is effective in vitro against
virtually all gram-negative pathogens, including 
Pseudomonas aeruginosa. It is also effective against gram-positive
pathogen such as staphylococci and 
streptococci. Anaerobes are generally less susceptible. 
 
Ciprofloxacin has a rapid bactericidal action, both in the
proliferation phase and in the resting phase. 
During the proliferation phase of a bacterium a segmental
twisting and untwisting of the chromosomes 
take place. An enzyme called DNA gyrase plays a decisive part in
this process. Ciprofloxacin inhibits 
this DNA gyrase in a way that arrests the bacterial metabolism,
since vital information can no longer 
be read from the bacterial chromosome. 
 
Resistance to ciprofloxacin develops slowly and in stages
(multiple-step type). Plasmid-mediated 
resistance development of the kind that occurs
with β-lactam antibiotics, aminoglycosides, and 
tetracyclines has not been observed with ciprofloxacin. It is of
clinical interest t
                                
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