1. COMPOSITION
Declared ingredients:
Norfloxacin HCl
Dexamethasone sodium phosphate
The old website has not published the specific concentration of each ingredient. The product label, registration dossier or official packshot should be checked before adding the concentrations.
2. INDICATIONS
Treatment of postpartum metritis in cattle, buffaloes, pigs, goats and sheep.
Treatment of vaginitis and uterine infections resulting from obstetric intervention during parturition.
The product's main claim is the treatment of vaginitis – metritis.
3. ADMINISTRATION & DOSAGE
Dip the tablet in clean water, then insert it deep into the animal's uterus. Continue treatment until purulent discharge is no longer present, then discontinue.
PIGS, GOATS AND SHEEP
Dosage: 1 tablet/time/day.
Route of administration: Insert deep into the uterus.
Duration of use: Continue administration until purulent discharge is no longer present, then discontinue.
CATTLE AND BUFFALOES
Dosage: 2 tablets/time/day.
Route of administration: Insert deep into the uterus.
Duration of use: Continue administration until purulent discharge is no longer present, then discontinue.
4. DOSAGE FORM / ROUTE OF USE
Dosage form: Intrauterine tablet.
Route of use: Insert directly into the uterus.
Preparation before use: Dip the tablet in clean water.
Product group: Antibiotic.
5. PRECAUTIONS
Dip the tablet in clean water before insertion and insert it deep into the animal's uterus.
Use the correct number of tablets corresponding to pigs, goats and sheep, or cattle and buffaloes.
The Vietnamese and English pages of the old website are not fully consistent regarding target species, prophylactic use and duration of administration. This CMS content prioritizes the instructions on the Vietnamese page.
Do not include prophylactic use for 2 - 3 days or a treatment course of 3 - 4 days in the CMS until confirmed by the current product label or registration dossier.
The current route-of-use filter does not include an “Intrauterine insertion” option; do not force the product into the “Direct infusion” option because ANTI-GATE is a tablet dosage form.
The old website has not published the concentration of each ingredient, withdrawal period, contraindications, storage conditions or packaging specifications. The product label, registration dossier or official packshot should be checked before adding this information.