Animal NDC 57926-477-07 Fertagyl

Gonadorelin

Animal Product Information

Field Name Field Value
Animal NDC Code 57926-477-07
Proprietary Name Fertagyl What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Gonadorelin What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Labeler Name Merck Sharp & Dohme Corp.
Product Type Prescription Animal Drug
Usage Information
    INDICATIONS FOR USE:
Active Ingredient(s)
  • Gonadorelin
Inactive Ingredient(s)
  • SODIUM CHLORIDE (451W47IQ8X)
  • SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (5QWK665956)
  • BENZYL ALCOHOL (LKG8494WBH)
  • WATER (059QF0KO0R)
  • SODIUM CHLORIDE (451W47IQ8X)
  • SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (5QWK665956)
  • BENZYL ALCOHOL (LKG8494WBH)
  • WATER (059QF0KO0R)
Marketing Category ANADA - ABBREVIATED NEW ANIMAL DRUG APPLICATION What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number ANADA200134 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Fertagyl Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Other



189979 R9

For treatment of cystic ovaries in dairy cattle

For use with Estrumate (cloprostenol injection) to synchronize estrous cycles to allow for fixed time artificial insemination (FTAI) in lactating dairy cows

For use with cloprostenol sodium to synchronize estrous cycles to allow for FTAI in beef cows

Cystic Ovaries

Fertagyl is indicated for the treatment of ovarian follicular cysts in dairy cattle. Ovarian cysts are nonovulated follicles with incomplete luteinization which result in nymphomania or irregular estrus.

Historically, cystic ovaries have responded to an exogenous source of LH such as human chorionic gonadotropin.

Fertagyl initiates release of endogenous LH to cause ovulation and luteinization.

Reproductive Synchrony

Fertagyl is indicated for use with Estrumate (cloprostenol injection) to synchronize estrous cycles to allow for fixed time artificial insemination (FTAI) in lactating dairy cows.

Fertagyl is indicated for use with cloprostenol sodium to synchronize estrous cycles to allow for FTAI in beef cows.

Cystic Ovaries

The intravenous or intramuscular dosage of Fertagyl is 86 mcg gonadorelin (2 mL) per cow.

Reproductive Synchrony

For lactating dairy cows, the intramuscular dosage of Fertagyl is 86 mcg gonadorelin (2 mL) per cow, used in reproductive synchrony programs similar to the following:

  • Administer the first Fertagyl injection (2 mL) on Day 0.
  • Administer 2 mL of Estrumate (500 mcg cloprostenol, as cloprostenol sodium) by intramuscular injection 6 to 8 days after the first Fertagyl injection.
  • Administer the second Fertagyl injection (2 mL) 30 to 72 hours after the Estrumate injection.
  • Perform FTAI 8 to 24 hours after the second Fertagyl injection, or inseminate cows on detected estrus using standard herd practices.
  • For beef cows, the intramuscular dosage of Fertagyl is 86 mcg gonadorelin (2 mL) per cow, used in reproductive synchrony programs similar to the following:

    • Administer the first Fertagyl injection (2 mL) on Day 0.
    • Administer 500 mcg cloprostenol (as cloprostenol sodium) by intramuscular injection 6 to 8 days after the first Fertagyl injection.
    • Administer the second Fertagyl injection (2 mL) 30 to 72 hours after the cloprostenol sodium injection.
    • Perform FTAI 0 to 24 hours after the second Fertagyl injection, or inseminate cows on detected estrus using standard herd practices.
    • WITHDRAWAL PERIODS:

      No withdrawal period or milk discard time is required when used according to the labeling.

      To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Intervet at 1-800-211-3573. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or http://www.fda.gov/reportanimalae.

      TARGET ANIMAL SAFETY:

      In addition to the animal safety information presented in the PHARMACOLOGY AND TOXICOLOGY section, the safety of gonadorelin was established through the review and evaluation of the extensive published literature available for the use of gonadorelin-containing products.

      The intramuscular administration of 860 mcg gonadorelin (as gonadorelin acetate) on five (5) consecutive days to normally cycling dairy cattle had no effect on hematology or clinical chemistries. In field studies evaluating the effectiveness of gonadorelin for the treatment of ovarian follicular cysts, the incidence of health abnormalities was not significantly greater in cows administered gonadorelin than cows administered a placebo injection.

      The target animal safety of, and injection site reactions to, Fertagyl when used with Estrumate (cloprostenol injection) were evaluated during the conduct of effectiveness field studies in lactating dairy cows. The incidence of health abnormalities was not significantly greater in cows administered Fertagyl than cows administered a placebo injection.

      The target animal safety of, and injection site reactions to, gonadorelin when used with cloprostenol sodium were evaluated during the conduct of effectiveness field studies in beef cows. The incidence of health abnormalities was not significantly greater in cows administered gonadorelin than cows administered a placebo injection.

      EFFECTIVENESS:

      The use of gonadorelin for treatment of ovarian follicular cysts in dairy cattle was demonstrated to be effective with a treatment dose of 86 mcg gonadorelin (as gonadorelin acetate).

      The effectiveness of Fertagyl for use with Estrumate (cloprostenol injection) to synchronize estrous cycles to allow for FTAI in lactating dairy cows was demonstrated in a field study at six different locations in the U.S. A total of 758 healthy, non-pregnant, primiparous or multiparous lactating dairy cows within 50-120 days postpartum were enrolled in the study. A total of 377 cows were administered Fertagyl (2 mL; 86 mcg gonadorelin as the acetate salt) and 381 cows were administered an equivalent volume of saline as an intramuscular injection twice in the following regimen:

      Day 0: 2 mL Fertagyl or saline
      Day 7: 2 mL Estrumate (cloprostenol injection)
      Day 9: 2 mL Fertagyl or saline

      Fixed time Al was performed on Day 10, 16 ± 8 hours after the Day 9 injection. Cows were evaluated for pregnancy on Day 45 ± 5 days by trans-rectal ultrasound or rectal palpation. Pregnancy rate to FTAI was significantly higher (P=0.0051) in cows treated with Fertagyl (33.4%) than the pregnancy rate to FTAI to cows treated with saline (17.8%).

      The effectiveness of gonadorelin for use with cloprostenol sodium to synchronize estrous cycles to allow for FTAI in beef cows was demonstrated in a field study at 10 different locations in the U.S. A total of 706 healthy, non-pregnant, primiparous or multiparous beef cows within 40-150 days postpartum were enrolled in the study. A total of 364 cows were administered gonadorelin (1 mL; 100 mcg gonadorelin as the acetate salt) and 342 cows were administered an equivalent volume of water for injection as an intramuscular injection twice in the following regimen:

      Day 0: 100 mcg gonadorelin (as the acetate salt) or sterile water for injection
      Day 7: 500 mcg cloprostenol (as cloprostenol sodium)
      Day 9: 100 mcg gonadorelin (as the acetate salt) or sterile water for injection

      Fixed time AI was performed immediately after the Day 9 injection. Cows were evaluated for pregnancy on Day 55±5 days by trans-rectal ultrasound. Pregnancy rate to FTAI was significantly higher (P=0.0006) in cows treated with gonadorelin (21.7%) than the pregnancy rate to FTAI in cows treated with water (7.4%).

      The effectiveness of a 2-mL dose of gonadorelin delivering 86 mcg gonadorelin (as gonadorelin acetate) for use with cloprostenol sodium to synchronize estrous cycles to allow for FTAI in lactating dairy cows and beef cows was also demonstrated through references to scientific literature.

      Approved by FDA under ANADA # 200-134
      Manufactured for:
      Intervet Inc. (d/b/a Merck Animal Health)
      Madison, NJ 07940
      Gonadorelin (active ingred.) made in the Netherlands. Formulated in Germany.

      Copyright©2020 Intervet Inc. (d/b/a Merck Animal Health), a subsidiary of Merck and Co., Inc.
      All rights reserved.

      Rev. 02/2020


Precautions



CAUTION:

Federal law restricts this drug to use by or on the order of a licensed veterinarian.


Description



DESCRIPTION:

Fertagyl is a sterile solution containing 43 mcg/mL of gonadorelin (GnRH: as gonadorelin acetate) suitable for intramuscular or intravenous administration according to the indication.

Gonadorelin is a decapeptide composed of the sequence of amino acids –

5-oxoPro-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2

a molecular weight of 1182.32 and empirical formula C55H75N17O13.

Each mL of Fertagyl contains:

Gonadorelin (as gonadorelin acetate)43 mcg
Benzyl Alcohol9 mg
Sodium Chloride7.47 mg
Water for Injection, USPq.s.

pH adjusted with sodium phosphate (monobasic and dibasic).

Gonadorelin is the hypothalamic releasing factor responsible for the release of gonadotropins (e.g., luteinizing hormone [LH], follicle stimulating hormone [FSH]) from the anterior pituitary.

Synthetic gonadorelin is physiologically and chemically identical to the endogenous bovine hypothalamic releasing factor.


Indications & Usage



INDICATIONS FOR USE:


Dosage & Administration



DOSAGE AND ADMINISTRATION:


Warnings



WARNINGS AND PRECAUTIONS:

Not for use in humans. Keep out of reach of children.


Animal Pharmacology & Or Toxicology



PHARMACOLOGY AND TOXICOLOGY:

Endogenous gonadorelin is synthesized and/or released from the hypothalamus during various stages of the bovine estrous cycle following appropriate neurogenic stimuli. It passes via the hypophyseal portal vessels, to the anterior pituitary to effect the release of gonadotropins (e.g. LH, FSH).

Synthetic gonadorelin administered intravenously or intramuscularly also causes the release of endogenous LH or FSH from the anterior pituitary.

Gonadorelin acetate has been shown to be safe. The LD50 for mice and rats is greater than 60 mg/kg, and for dogs, greater than 600 mcg/kg, respectively. No adverse effects were noted among rats or dogs administered 120 mcg/kg/day or 72 mcg/kg/day intravenously for 15 days.

It had no adverse effects on heart rate, blood pressure, or EKG to unanesthetized dogs at 60 mcg/kg. In anesthetized dogs it did not produce depression of myocardial or system hemodynamics or adversely affect coronary oxygen supply or myocardial oxygen requirements.

The intravenous administration of 60 mcg/kg/day gonadorelin acetate to pregnant rats and rabbits during organogenesis did not cause embryotoxic or teratogenic effects.

Further, gonadorelin acetate did not cause irritation at the site of intramuscular administration in dogs with a dose of 72 mcg/kg/day administered for seven (7) days.


How Supplied



HOW SUPPLIED:

Fertagyl is available in a concentration of 43 mcg/mL gonadorelin (as gonadorelin acetate) pH adjusted with sodium phosphate (monobasic and dibasic).

Fertagyl is supplied in multi-dose vials containing 20 mL and 100 mL of sterile solution.


Storage And Handling



STORAGE, HANDLING, AND DISPOSAL: Keep refrigerated: 2°-8°C (36°-46°F).

20 mL vial: Use within 28 days of first puncture.

100 mL vial: Use within 28 days of first puncture and puncture a maximum of 10 times when using an 18 gauge needle. When using a draw-off spike or needle with bore diameter larger than 18 gauge, discard any product remaining in the vial immediately after use.


Principal Display Panel - 20 Ml Vial Carton



MERCK
Animal Health

20 mL

fertagyl®
(gonadorelin)
43 mcg/mL gonadorelin Injectable Solution

INDICATIONS FOR USE:
For the treatment of cystic ovaries in
dairy cattle.
For use with Estrumate (cloprostenol
injection) to synchronize estrous cycles to
allow for fixed time artificial insemination
(FTAI) in lactating dairy cows.
For use with cloprostenol sodium to
synchronize estrous cycles to allow
for FTAI in beef cows.

CAUTION: Federal law restricts this drug
to use by or on the order of a licensed veterinarian.

Approved by FDA under ANADA # 200-134

Net Contents:
20 mL/10 doses

MERCK
Animal Health


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.