SWINEMATE- altrenogest solution

SwineMate by

Drug Labeling and Warnings

SwineMate by is a Animal medication manufactured, distributed, or labeled by Aurora Pharmaceutical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Solution 0.22% (2.2 mg/mL)

FOR USE IN ANIMALS ONLY

Approved by FDA under ANADA # 200-621

Restricted Drug (California) — use only as directed. Not for Human Use

DRUG FACTS:

Active Ingredients: Altrenogest solution 0.22% (2.2 mg/mL)

WHEN USING

Use: For synchronization of estrus in sexually mature gilts that have had at least one estrous cycle. Treatment with altrenogest solution 0.22% results in estrus (standing heat) 4 to 9 days after completion of the 14-day treatment period.

DO NOT USE

Caution: Federal law prohibits extra-label use of this drug to enhance food and/or fiber production in animals.

DO NOT USE

Do Not Use: In gilts having a previous or current history of uterine inflammation (i.e., acute, subacute or chronic endometritis).

WARNINGS:

User/Handler Safety: Keep this and all medication out of the reach of children.

Avoid skin contact. Wear vinyl, neoprene or nitrile protective gloves when handling this product.
DO NOT USE LATEX GLOVES. Pregnant women or women who suspect they are pregnant should not handle SwineMate® (altrenogest) Solution 0.22%. Women of childbearing age should exercise extreme caution when handling this product. Accidental absorption could lead to a disruption of the menstrual cycle or prolongation of pregnancy. Wash off accidental spillage on the skin immediately with soap and water.

People who should not handle this product:
1. Women who are or suspect they are pregnant.
2. Anyone with thrombophlebitis or thromboembolic disorders or with a history of these events.
3. Anyone with cerebral-vascular or coronary-artery disease.
4. Women with known or suspected carcinoma of the breast.
5. People with known or suspected estrogen-dependent neoplasia.
6. Women with undiagnosed vaginal bleeding.
7. People with benign or malignant tumors which developed during the use of oral contraceptives or other estrogen-containing products.
8. Anyone with liver dysfunction or disease.

Accidental exposure: Altrenogest is readily absorbed from contact with the skin. In addition, this oil-based product can penetrate porous gloves. Altrenogest should not penetrate intact vinyl, neoprene or nitrile protective gloves; however, if there is leakage (i.e., pinhole, spillage, etc.) the contaminated area covered by such occlusive materials may have increased absorption.
DO NOT USE LATEX GLOVES.

The following measures are recommended in case of accidental exposure.
Skin Exposure: Wash immediately with soap and water.
Eye Exposure: Immediately flush with plenty of water for 15 minutes. Get medical attention.
If Swallowed: Do not induce vomiting. SwineMate® (altrenogest) Solution 0.22% contains an oil. Call a physician. Vomiting should be supervised by a physician because of possible pulmonary damage via aspiration of the oil base. If possible, bring the container and labeling to the physician.

Effects of Overexposure: There has been no human use of this specific product. The information contained in this section is extrapolated from data available on other products of the same pharmacological class that have been used in humans. Effects anticipated are due to the progestational activity of altrenogest. Acute effects after a single exposure are possible; however, continued daily exposure has the potential for more untoward effects such as disruption of the menstrual cycle, uterine or abdominal cramping, increased or decreased uterine bleeding, prolongation of pregnancy and headaches. The oil base may also cause complications if swallowed. In addition, the list of people who should not handle this product is based upon the known effects of progestins used in humans on a chronic basis.

FOOD SAFETY WARNING

Human Food Safety: Gilts must not be slaughtered for

human consumption for 21 days after the last treatment

OTHER SAFETY INFORMATION

Environmental Safety: Place empty drug containers and used syringes, protective gloves or other articles that come in contact with this product in a leak-resistant container for disposal in accordance with applicable Federal, state and local regulations.

ADVERSE REACTIONS

Adverse Reactions and Potential Safety Hazards: Underfeeding of SwineMate® may lead to the occurrence of cystic follicles.

WHEN USING

When Using This Product: A small percentage (less than 5%) of treated gilts may exhibit estrus (standing heat) during the 14-day treatment period. Gilts nearing estrus at the start of the 14-day treatment period may express estrus early in that period.

DOSAGE & ADMINISTRATION

Dosage and Directions: While wearing protective gloves, remove shipping cap and seal; replace with enclosed plastic dispensing cap. Remove cover from bottle dispensing tip and connect luer lock syringe (without needle). Draw out appropriate volume of SwineMate® solution. (Note: Do not remove syringe while bottle is inverted as spillage may result.) Detach syringe and replace cover on bottle dispensing tip to prevent leakage. Administer 6.8 mL (15 mg altrenogest) per gilt once daily for 14 consecutive days. Treat gilts on an individual animal basis by top-dressing SwineMate® on a portion of each gilt’s daily feed allowance. To produce the desired synchronization of estrus in a group of gilts, treat all of the gilts daily for the same 14-day period.

Excessive use of a syringe may cause the syringe to stick; therefore, replace syringe as necessary.

OTHER INFORMATION:

Storage: Store at or below room temperature, 77° F (25° C). Close tightly.

QUESTIONS? COMMENTS?
To report a suspected adverse reaction, call 888-215-1256.
To obtain product information, including safety data sheet (SDS), call 888-215-1256.

For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at http://www.fda.gov/AnimalVeterinary/SafetyHealth

MANUFACTURED IN THE USA

REORDER NO: 22000

Manufactured by:
Aurora Pharmaceutical, Inc.
NORTHFIELD, MN 55057
888-215-1256
www.aurorapharmaceutical.com
IN 50-1408   02/2019

NDC: 51072-086-00

Net Contents: 1000 mL

Container Label

PRINCIPAL DISPLAY PANEL - 1000 mL bottle label

Warning Shipper Label

INGREDIENTS AND APPEARANCE

SWINEMATE 
altrenogest solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 51072-086
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: 51072-086-00	1000 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANADA	ANADA200621	08/02/2017

Labeler - Aurora Pharmaceutical, Inc. (832848639)

Establishment
Name	Address	ID/FEI	Business Operations
Aurora Pharmaceutical, Inc.		832848639	manufacture