Label: MATE- altrenogest solution
- NDC Code(s): 51072-119-00
- Packager: Aurora Pharmaceutical, Inc.
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated September 6, 2023
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- DOSAGE FORMS & STRENGTHS
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VETERINARY INDICATIONS
For regulation and control of the breeding cycle of mares
• To induce ovulatory oestrus early in the breeding season in mares where some follicular activity exists
• For the suppression of oestrus either during prolonged oestrus or in normally cycling mares
• For the control of the ovarian cycle in breeding mares to allow the most efficient use of the stallionFor the maintenance of pregnancy in habitually aborting mares, or mares at risk of early embryonic death or abortion, where progesterone deficiency is thought to be the underlying cause.
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CONTRAINDICATIONS
Read the carton for full instruction
DIRECTIONS FOR USE
Restraints:
DO NOT USE on male animals.Contraindications:
Contraindicated for use in mares suffering from uterine infections.Precautions:
Use with caution as unused feed must be destroyed and not given to any other animals.
MATE must be added to the feed immediately prior to consumption and not stored. -
Dosage and Administration:
For oral administration.
Administer 1 mL MATE per 50 kg bodyweight (equivalent to 0.044 mg altrenogest per kg) daily.
1. Regulation and control of the breeding cycle of mares
a. For the induction of ovulatory oestrus or to induce cyclical ovarian activity in mares with some follicle activity early in the breeding season: Administer MATE daily for 10 consecutive days.
b. For the suppression of oestrus in normally cycling mares: Administer MATE daily for 15 consecutive days. For the suppression of prolonged oestrus: Administer MATE daily for 10 consecutive days.
c. To control the breeding cycle of mares to allow efficient use of the stallion: Administer MATE daily for 15 consecutive days.
2. For the treatment of habitually aborting mares, or mares at risk of early embryonic death or abortion: Administer MATE daily, from the 2nd or 3rd day after ovulation in the mated or inseminated mare, continuing until day 120 of gestation.NOTE: Ultrasound scanning to confirm pregnancy is recommended on day 14 or 15 after ovulation. If the mare is not pregnant, it is advised to cease MATE administration and to administer an injection of prostaglandin F2α to destroy any luteal tissue that may be still present, allowing the mare to return to oestrus and be re-mated.
MEAT WITHHOLDING PERIODS (HORSES)
DO NOT USE less than 28 days before slaughter for human consumption.
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SAFETY DIRECTIONS
Product is harmful if absorbed by skin contact, inhaled or swallowed. Avoid contact with eyes and skin. Do not inhale. When using the product wear rubber gloves. After use and before eating, drinking or smoking, wash hands, arms and face thoroughly with soap and water. After each day's use, wash gloves. Care should be taken to avoid contact between the solution and women of child bearing age.
FIRST AID INSTRUCTIONS
If poisoning occurs, contact a doctor or Poisons Information Centre. Phone Australia 13 11 26.ADDITIONAL USER SAFETY INFORMATION
Additional information is listed in the safety data sheet (SDS). - STORAGE
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MATE
altrenogest solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:51072-119 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALTRENOGEST (UNII: 2U0X0JA2NB) (ALTRENOGEST - UNII:2U0X0JA2NB) ALTRENOGEST 2.2 mg in 1 mL Product Characteristics Color yellow (colorless to yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51072-119-00 1000 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 09/01/2023 Labeler - Aurora Pharmaceutical, Inc. (832848639) Establishment Name Address ID/FEI Business Operations Aurora Pharmaceutical, Inc. 832848639 manufacture