ESTROPLAN- cloprostenol sodium injection, solution United States - English - NLM (National Library of Medicine)

estroplan- cloprostenol sodium injection, solution

parnell technologies pty ltd - cloprostenol sodium (unii: 886sav9675) (cloprostenol - unii:4208238832) - cloprostenol 250 ug in 1 ml - approved by fda under anada # 200-310 estroplan (cloprostenol sodium) prostaglandin analogue for cattle equivalent to 250 mcg cloprostenol/ml caution: federal law restricts this drug to use by or on the order of a licensed veterinarian. description: estroplan (cloprostenol sodium) is a synthetic prostaglandin analogue structurally related to prostaglandin f2 α (pgf2 α ). each ml of the colorless aqueous solution contains 263 mcg of cloprostenol sodium (equivalent to 250 mcg of cloprostenol), chlorocresol 1.0 mg as a bactericide, citric acid anhydrous 0.66 mg, sodium citrate 5.03 mg, sodium chloride 6.76 mg. the ph is adjusted, as necessary, with sodium hydroxide or citric acid. action: estroplan causes functional and morphological regression of the corpus luteum (luteolysis) in cattle. in normal, nonpregnant cycling animals this effect on the life span of the corpus luteum usually results in estrus 2 to 5 days after treatment. in animals with prolonged luteal function (pyometra, mummified fetus, and

SYNCHSURE- cloprostenol sodium injection, solution United States - English - NLM (National Library of Medicine)

synchsure- cloprostenol sodium injection, solution

merial, inc. - cloprostenol sodium (unii: 886sav9675) (cloprostenol - unii:4208238832) - cloprostenol 250 ug in 1 ml - indications: for intramuscular use to induce luteolysis in beef and dairy cattle. the luteolytic action of synchsure can be utilized to manipulate the estrous cycle to better fit certain management practices, to terminate pregnancies resulting from mismatings, and to treat certain conditions associated with prolonged luteal function. contraindications: synchsure should not be administered to a pregnant animal whose calf is not to be aborted.

ESTRUMATE- cloprostenol sodium injection United States - English - NLM (National Library of Medicine)

estrumate- cloprostenol sodium injection

merck sharp & dohme corp. - cloprostenol sodium (unii: 886sav9675) (cloprostenol - unii:4208238832) - - for unobserved or non-detected estrus in beef cows, lactating dairy cows, and replacement beef and dairy heifers - for treatment of pyometra or chronic endometritis in beef cows, lactating dairy cows, and replacement beef and dairy heifers - for treatment of mummified fetus in beef cows, lactating dairy cows, and replacement beef and dairy heifers - for treatment of luteal cysts in beef cows, lactating dairy cows, and replacement beef and dairy heifers - for abortion of beef cows, lactating dairy cows, and replacement beef and dairy heifers - for estrus synchronization in beef cows, lactating dairy cows, and replacement beef and dairy heifers - for use with fertagyl® (gonadorelin) to synchronize estrous cycles to allow for fixed time artificial insemination (ftai) in lactating dairy cows. estrumate causes functional and morphological regression of the corpus luteum (luteolysis) in cattle. in normal, non-pregnant cycling animals, this effect on the life span of the corpus luteum usually results in estrus

SYNCHSURE- cloprostenol sodium injection, solution United States - English - NLM (National Library of Medicine)

synchsure- cloprostenol sodium injection, solution

boehringer ingelheim animal health usa inc. - cloprostenol sodium (unii: 886sav9675) (cloprostenol - unii:4208238832) - indications: for intramuscular use to induce luteolysis in beef and dairy cattle. the luteolytic action of synchsure can be utilized to manipulate the estrous cycle to better fit certain management practices, to terminate pregnancies resulting from mismatings, and to treat certain conditions associated with prolonged luteal function. contraindications: synchsure should not be administered to a pregnant animal whose calf is not to be aborted.

CLOPROSTENOL SODIUM powder United States - English - NLM (National Library of Medicine)

cloprostenol sodium powder

everlight chemical industrial corporation kuanyin ii plant - cloprostenol sodium (unii: 886sav9675) (cloprostenol - unii:4208238832) -

Cloprostenol sodium Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

cloprostenol sodium

syntex s.a. - cloprostenol sodium - unknown - cloprostenol sodium prostaglandin active 0.0 - active constituent

CLOPROSTENOL SODIUM Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

cloprostenol sodium

jurox pty limited - cloprostenol sodium - unknown - cloprostenol sodium prostaglandin active 0.0 - active constituent

CLOPROSTENOL VEYX SW SOLUTION Canada - English - Health Canada

cloprostenol veyx sw solution

modern veterinary therapeutics llc - cloprostenol (cloprostenol sodium) - solution - 175mcg - cloprostenol (cloprostenol sodium) 175mcg - swine (pigs)

CLOPROSTENOL VEYX SOLUTION Canada - English - Health Canada

cloprostenol veyx solution

modern veterinary therapeutics llc - cloprostenol (cloprostenol sodium) - solution - 0.25mg - cloprostenol (cloprostenol sodium) 0.25mg - cattle

ESTRUMATE- cloprostenol injection United States - English - NLM (National Library of Medicine)

estrumate- cloprostenol injection

merck sharp & dohme corp. - cloprostenol (unii: 4208238832) (cloprostenol - unii:4208238832) - for intramuscular use to induce luteolysis in beef and dairy cattle. the luteolytic action of estrumate can be utilized to manipulate the estrous cycle to better fit certain management practices, to terminate pregnancies resulting from mismatings, and to treat certain conditions associated with prolonged luteal function. cows which are not detected in estrus, although ovarian cyclicity continues, can be treated with estrumate if a mature corpus luteum is present. estrus is expected to occur 2 to 5 days following injection, at which time animals may be inseminated. treated cattle should be inseminated at the usual time following detection of estrus. if estrous detection is not desirable or possible, treated animals may be inseminated twice at about 72 and 96 hours postinjection. damage to the reproductive tract at calving or postpartum retention of the placenta often leads to infection and inflammation of the uterus (endometritis). under certain circumstances, this may progress into chronic endometritis with