Label: VENTIPULMIN- clenbuterol syrup
- NDC Code(s): 0010-3017-02, 0010-3017-03
- Packager: Boehringer Ingelheim Animal Health USA Inc.
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Animal Drug Application
Drug Label Information
Updated June 8, 2022
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Caution:
- Each mL contains:
-
Description:
Clenbuterol (4-amino-alpha-[(tert-butylamino) methyl]-3, 5-dichlorobenzyl alcohol hydrochloride) is a beta-2-adrenergic agonist which provides bronchodilating properties as well as other effects, with minimum effect on the cardiovascular system. It is provided as a colorless, palatable syrup. VENTIPULMIN Syrup (clenbuterol hydrochloride) is antagonized by beta-adrenergic blocking agents.
- Indications:
- Contraindications:
- Warning:
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Human Warnings:
Not for use in humans. Do not use in horses intended for human consumption. Keep out of reach of children. In case of accidental ingestion, contact a physician immediately. Ingestion of VENTIPULMIN Syrup may cause undesirable reactions. Clenbuterol, like other beta adrenergic agonists, can produce significant cardiovascular effects in some people as evidenced by elevated pulse rate, blood pressure changes and/or ECG changes.
- Dosage and Administration:
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Dosage Schedule:
Initial dosage: administer 0.5 mL/100 lbs (0.8 mcg/kg) for 3 days (6 treatments); If no improvement, administer 1.0 mL/100 lbs (1.6 mcg/kg) for 3 days (6 treatments); If no improvement, administer 1.5 mL/100 lbs (2.4 mcg/kg) for 3 days (6 treatments); If no improvement, administer 2.0 mL/100 lbs (3.2 mcg/kg) for 3 days (6 treatments); If no improvement, horse is non-responsive to clenbuterol and treatment should be discontinued. Recommended duration of treatment at effective dose is 30 days. At the end of this 30-day treatment period, drug should be withdrawn to determine recurrence of signs. If signs return, the 30-day treatment regimen may be repeated. If repeating treatment, the step-wise dosage schedule should be repeated.
- Directions for Administration:
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Dosage Calculation Chart
Lbs. Body
Weight
mL/treatment
at 0.5 mL/100#
(0.8 mcg/kg)
mL/treatment
at 1.0 mL/100#
(1.6 mcg/kg)
mL/treatment
at 1.5 mL/100#
(2.4 mcg/kg)
mL/treatment
at 2.0 mL/100#
(3.2 mcg/kg)
500
600
700
800
900
1000
1100
1200
1300
1400
1500
1600
1700
1800
2.5
3.0
3.5
4.0
4.5
5.0
5.5
6.0
6.5
7.0
7.5
8.0
8.5
9.0
5.0
6.0
7.0
8.0
9.0
10.0
11.0
12.0
13.0
14.0
15.0
16.0
17.0
18.0
7.5
9.0
10.5
12.0
13.5
15.0
16.5
18.0
19.5
21.0
22.5
24.0
25.5
27.0
10.0
12.0
14.0
16.0
18.0
20.0
22.0
24.0
26.0
28.0
30.0
32.0
34.0
36.0
Administer two treatments per day.
- Precaution:
-
Adverse Reactions:
Mild sweating, muscle tremor, restlessness, urticaria and tachycardia may be observed in some horses during the first few days of treatment. May cause elevated creatine kinase (CK) serum levels. Ataxia was observed in 3 out of 239 horses (1.3%) in clinical studies. To report suspected adverse events, for technical assistance, or to obtain a copy of the Safety Data Sheet (SDS), contact Boehringer Ingelheim Animal Health USA Inc. at 1-888-637-4251. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at www.fda.gov/reportanimalae.
- How Supplied:
- Storage:
- SPL UNCLASSIFIED SECTION
- Principal Display Panel – 330 mL Container Label
-
Principal Display Panel – 330 mL Display Carton – Front and Side Panel
NDC 0010-3017-03
Ventipulmin® Syrup
Clenbuterol HCl 72.5 mcg/mL
Caution: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Caution: Federal law prohibits the extralabel use of this drug in food animals.
For oral use in horses only
Approved by FDA under NADA # 140-973
- Principal Display Panel - 330 mL Display Carton – Back and Side Panel
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INGREDIENTS AND APPEARANCE
VENTIPULMIN
clenbuterol syrupProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:0010-3017 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLENBUTEROL HYDROCHLORIDE (UNII: GOR5747GWU) (CLENBUTEROL - UNII:XTZ6AXU7KN) CLENBUTEROL HYDROCHLORIDE 0.0725 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0010-3017-02 1 in 1 CARTON 1 100 mL in 1 BOTTLE, PLASTIC 2 NDC:0010-3017-03 1 in 1 CARTON 2 330 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NADA NADA140973 01/12/2011 Labeler - Boehringer Ingelheim Animal Health USA Inc. (007134091)