01 2ACS DOBFAR SPA
02 2Actavis Inc
03 1Antibiotice SA
04 2Aurobindo Pharma Limited
05 1Austell Laboratories
06 1Bernofarm Pharmaceutical Company
07 2Brooks laboratories Limited
08 2Fresenius SE & Co. KGaA
09 1HQ SPCLT PHARMA
10 3Health Biotech
11 1Hikma Pharmaceuticals
12 5Hospira, Inc.
13 1Jeil Pharmaceutical Co., Ltd
14 1Jodas Expoim Pvt. Ltd
15 1MSD INTL GMBH
16 9Merck & Co
17 1Myungmoon Pharm. Co., LTD.
18 1ORIFARM GROUP AS
19 1Pharma Dynamics
20 2Sandoz B2B
21 4Sun Pharmaceutical Industries Limited
22 1Tamrisa
23 1Teva Pharmaceutical Industries
01 4INF
02 3INJ
03 2INJECTABLE;INJECTION
04 1INJECTION
05 1INJECTION;
06 1Imipenem+Cilastatin+500500 Mg 1 Unit Parenteral Use
07 2Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
08 1Imipenem+Cilastatin+500500 Mg 20Ml 1 Units Parenteral Use
09 1Imipenem+Cilastatin+500500 Mg 20Ml 5 Units Parenteral Use
10 1Imipenem+Cilastatin+500500 Mg 30Ml 1 Units Parenteral Use
11 4Injection
12 4POWDER FOR SOLUTION
13 2POWDER;INTRAMUSCULAR
14 9POWDER;INTRAVENOUS
15 1Powder for Injection
16 4Powder for infusion fluid, resolution
17 3Vial
18 1powder for injection/Infusion
19 1Blank
01 8DISCN
02 9Generic
03 1Originator
04 5RX
05 23Blank
01 1 Imipenem Cilastatine Tamrisa®
02 1ACTAPEN 500
03 1Cilapen 500
04 6IMIPENEM AND CILASTATIN
05 2IMIPENEM AND CILASTATIN FOR INJECTION USP
06 2IMIPENEM/CILASTATIN 500MG/500MG FRESENIUS
07 1IMIPENEM/CILASTATIN Atb®
08 1IMIPEX
09 1Imcil 500mg**
10 1Imecitin
11 3Imipenem And Cilastatin
12 1Imipenem Cilastatin
13 1Imipenem/Cilastatin Actavis
14 1Imipenem/Cilastatin Hospira
15 6PRIMAXIN
16 1RECARBRIO
17 1Sepencil 500 mg
18 2TARO-IMIPENEM-CILASTATIN
19 3Tienam
20 1Tienam 500
21 1Tipem
22 8Blank
01 4Canada
02 1France
03 1Georgia
04 7India
05 6Italy
06 4Norway
07 1Romania
08 7South Africa
09 2South Korea
10 13USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPENEM AND CILASTATIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL
Packaging :
Approval Date : 2011-12-21
Application Number : 90577
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPENEM AND CILASTATIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 2011-12-21
Application Number : 90577
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem And Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
Dosage Strength : 10 VIALS EV 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Imipenem/Cilastatin Actavis
Dosage Form : Powder for infusion fluid, resolution
Dosage Strength : 500 mg/500 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 250MG; 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : Italy
Brand Name : Imecitin
Dosage Form : Imipenem+Cilastatin+500500 Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Georgia
Brand Name : IMIPEX
Dosage Form : Injection
Dosage Strength : 1G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Georgia
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 500MG
Packaging : Vial
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 1000MG
Packaging : Vial
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem And Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
Dosage Strength : 10 vials soluz Chk 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPENEM AND CILASTATIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL
Packaging :
Approval Date : 2011-11-16
Application Number : 90825
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPENEM AND CILASTATIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 2011-11-16
Application Number : 90825
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : IMIPENEM AND CILASTATIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 2011-11-16
Application Number : 91007
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 20Ml 5 Units Parenteral Use
Dosage Strength : 5 VIALS EV 500 mg + 500 mg 20 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Imipenem/Cilastatin Hospira
Dosage Form : Powder for infusion fluid, resolution
Dosage Strength : 500 mg/500 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : RX
Registration Country : USA
Brand Name : IMIPENEM AND CILASTATIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 2019-12-12
Application Number : 207594
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Korea
Brand Name :
Dosage Form : INJECTION;
Dosage Strength : 0.5MG; 0.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 250MG; 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMAXIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-11-26
Application Number : 50587
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMAXIN
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 1985-11-26
Application Number : 50587
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMAXIN
Dosage Form : POWDER;INTRAMUSCULAR
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 1990-12-14
Application Number : 50630
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMAXIN
Dosage Form : POWDER;INTRAMUSCULAR
Dosage Strength : EQ 750MG BASE/VIAL;750MG/VIAL
Packaging :
Approval Date : 1990-12-14
Application Number : 50630
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMAXIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL
Packaging :
Approval Date : 1987-01-08
Application Number : 62756
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMAXIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL
Packaging :
Approval Date : 1987-01-08
Application Number : 62756
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Italy
Brand Name : Tienam
Dosage Form : Imipenem+Cilastatin+500500 Mg 20Ml 1 Units Parenteral Use
Dosage Strength : 1 vial soluz Chk 500 mg + 500 mg 20 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Tienam
Dosage Form : Powder for infusion fluid, resolution
Dosage Strength : 500 mg/500 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : RX
Registration Country : USA
CILASTATIN SODIUM; IMIPENEM; RELEBACTAM
Brand Name : RECARBRIO
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL;250MG/VIAL
Packaging :
Approval Date : 2019-07-16
Application Number : 212819
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Korea
Brand Name : Tipem
Dosage Form : INJECTION
Dosage Strength : 530MG; 532MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info :
Registration Country : Norway
Brand Name : Tienam
Dosage Form : Powder for infusion fluid, resolution
Dosage Strength : 500 mg/500 mg
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Italy
Brand Name : Imipenem And Cilastatin
Dosage Form : Imipenem+Cilastatin+500500 Mg 30Ml 1 Units Parenteral Use
Dosage Strength : 1 vial EV 30 ml 500 mg + 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
