Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 6Sanofi
02 1Amphastar Pharmaceuticals
03 2Aurobindo Pharma Limited
04 1B. Braun Medical
05 5Baxter Healthcare Corporation
06 3Caplin Point Laboratories Limited
07 2Flagship Biotech International Pvt. Ltd
08 1Fresenius Kabi Austria
09 1Fresenius Kabi USA
10 3GLAND PHARMA LIMITED
11 1Health Biotech
12 11Hikma Pharmaceuticals
13 5Hospira, Inc.
14 1Lunan Pharmaceutical
15 1MARCAN PHARMACEUTICALS INC
16 1Meitheal Pharmaceuticals
17 1Montage Laboratories
18 1Stragen Pharma SA
19 1Viatris
20 1Wockhardt
21 2Woodward Pharma Services
22 1Yangtze River Pharmaceutical Group
01 2Ampoule
02 1Concentrate for Solution for Infusion
03 1INJECTABLE; INJECTION
04 39INJECTABLE;INJECTION
05 1Injectable Solution
06 2Injectable; Injection
07 3Injection
08 1Liquid Injection
09 2SOLUTION
01 1Authorized
02 19DISCN
03 2Generic
04 2Prescription
05 20RX
06 8Blank
01 1Corotrope
02 18MILRINONE LACTATE
03 5MILRINONE LACTATE IN DEXTROSE 5%
04 12MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
05 2MILRINONE LACTATE IN PLASTIC CONTAINER
06 1MILRINONE LACTATE INJECTION USP
07 1MILRINONE LACTATE INJECTION, USP
08 1Milrinone Lactate
09 1PRIMACOR
10 4PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER
11 6Blank
01 2Canada
02 1China
03 5India
04 1Spain
05 42USA
06 1Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMACOR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1987-12-31
Application Number : 19436
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1994-08-09
Application Number : 20343
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 15MG BASE/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1994-08-09
Application Number : 20343
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1994-08-09
Application Number : 20343
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMACOR IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/200ML (EQ 0.2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1994-08-09
Application Number : 20343
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Corotrope
Dosage Form : Injectable Solution
Dosage Strength : 1MG
Packaging :
Approval Date : 1990-11-01
Application Number : 58849
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-08-02
Application Number : 76013
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)
Packaging :
Approval Date : 2002-05-28
Application Number : 75834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/200ML (EQ 0.2MG BASE/ML)
Packaging :
Approval Date : 2002-05-28
Application Number : 75834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-05-28
Application Number : 75936
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)
Packaging :
Approval Date : 2002-05-28
Application Number : 75510
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-05-28
Application Number : 75530
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-05-28
Application Number : 75660
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : Injectable; Injection
Dosage Strength : EQ 20MG /20ML (1MG/ML)
Packaging :
Approval Date :
Application Number : 75660
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : Injectable; Injection
Dosage Strength : EQ 50MG /50ML (1MG/ML)
Packaging :
Approval Date :
Application Number : 75660
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-05-28
Application Number : 75852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-05-28
Application Number : 75830
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2002-05-28
Application Number : 75884
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)
Packaging :
Approval Date : 2002-05-28
Application Number : 75885
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/200ML (EQ 0.2MG BASE/ML)
Packaging :
Approval Date : 2002-05-28
Application Number : 75885
Regulatory Info : DISCN
Registration Country : USA
