01 1ABEX Pharmaceutica
02 2ACS DOBFAR SPA
03 2Actavis Inc
04 1Antibiotice SA
05 2Aurobindo Pharma Limited
06 1Austell Laboratories
07 1Bernofarm Pharmaceutical Company
08 2Brooks laboratories Limited
09 2Fresenius SE & Co. KGaA
10 1HQ SPCLT PHARMA
11 3Health Biotech
12 1Hikma Pharmaceuticals
13 5Hospira, Inc.
14 1Jeil Pharmaceutical Co., Ltd
15 1Jodas Expoim Pvt. Ltd
16 1MSD INTL GMBH
17 1Macleods Pharmaceuticals Limited
18 9Merck & Co
19 1Myungmoon Pharm. Co., LTD.
20 1ORIFARM GROUP AS
21 1Pharma Dynamics
22 2RANBAXY LABORATORIES LIMITED
23 2Sandoz B2B
24 2Sun Pharmaceutical Industries Limited
25 1Tamrisa
26 1Teva Pharmaceutical Industries
01 4INF
02 5INJ
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 11Generic
03 1Originator
04 4Prescription
05 5RX
06 19Blank
01 1 Imipenem Cilastatine Tamrisa®
02 1ACTAPEN 500
03 1CILNEM
04 1Cilapen 500
05 6IMIPENEM AND CILASTATIN
06 2IMIPENEM AND CILASTATIN FOR INJECTION USP
07 2IMIPENEM/CILASTATIN 500MG/500MG FRESENIUS
08 1IMIPENEM/CILASTATIN Atb®
09 1IMIPEX
10 1Imcil 500mg**
11 1Imecitin
12 3Imipenem And Cilastatin
13 1Imipenem Cilastatin
14 1Imipenem/Cilastatin Actavis
15 1Imipenem/Cilastatin Hospira
16 6PRIMAXIN
17 1RECARBRIO
18 1Sepencil 500 mg
19 2TARO-IMIPENEM-CILASTATIN
20 1TIASEP
21 3Tienam
22 1Tienam 500
23 1Tipem
24 8Blank
01 4Canada
02 1France
03 1Georgia
04 7India
05 6Italy
06 4Norway
07 1Romania
08 9South 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
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