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01 2Shamrock Pharmachemi
02 1ABEX Pharmaceutica
03 2ACS DOBFAR SPA
04 2Actavis Inc
05 1Adcock Ingram
06 1Antibiotice
07 1Apta Medica Internacional d.o.o
08 3Associated Biotech
09 2Aurobindo Pharma Limited
10 1Austell Laboratories
11 1Bernofarm Pharmaceutical Company
12 2Brooks laboratories Limited
13 1Campus Pharma AB
14 2Central Procurement & Supplies Unit
15 2ELC Group
16 1Eugia Pharma
17 3Fresenius Kabi AB Brunna
18 2Fresenius SE & Co. KGaA
19 1HQ SPCLT PHARMA
20 3Health Biotech
21 1Hikma Pharmaceuticals
22 5Hospira, Inc.
23 1Jeil Pharmaceutical Co., Ltd
24 1Jodas Expoim Pvt. Ltd
25 1Karo Pharma
26 1Labatec Pharm
27 1MEDOCHEMIE LTD
28 1MSD INTL GMBH
29 1Macleods Pharmaceuticals Limited
30 1Medartuum
31 1Medreg
32 1Mepha Pharma
33 12Merck & Co
34 1Montage Laboratories
35 1Myungmoon Pharm. Co., LTD.
36 2ORIFARM GROUP AS
37 2Pfizer Inc
38 1Pharma Dynamics
39 1RANBAXY LABORATORIES LIMITED
40 4Sandoz B2B
41 1Steriscience
42 1Stravencon
43 4Sun Pharmaceutical Industries Limited
44 1Tamrisa
45 2Teva Pharmaceutical Industries
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01 3Dry Powder Injectable
02 1Dry Powder Injection
03 5INF
04 5INJ
05 2INJECTABLE;INJECTION
06 1INJECTION
07 1INJECTION;
08 1Imipenem+Cilastatin+500500 Mg 1 Unit Parenteral Use
09 2Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use
10 1Imipenem+Cilastatin+500500 Mg 20Ml 1 Units Parenteral Use
11 1Imipenem+Cilastatin+500500 Mg 20Ml 5 Units Parenteral Use
12 1Imipenem+Cilastatin+500500 Mg 30Ml 1 Units Parenteral Use
13 4Injection
14 4POWDER FOR SOLUTION
15 2POWDER;INTRAMUSCULAR
16 9POWDER;INTRAVENOUS
17 1Powder For Concentrate For Solution For Infusion
18 11Powder For Solution For Infusion
19 1Powder for Injection
20 4Powder for infusion fluid, resolution
21 16Solution For Injection
22 2Sterile Vial
23 3Vial
24 1powder for injection/Infusion
25 1Blank
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01 2Allowed
02 5Approved
03 4Authorised
04 2Authorized
05 3Cancelled
06 8DISCN
07 10Deregistered
08 12Generic
09 1Originator
10 4Prescription
11 5RX
12 2Withdrawn
13 25Blank
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01 1 Imipenem Cilastatine Tamrisa®
02 1ACTAPEN 500
03 1CILNEM
04 1Campenam
05 1Cilapen 500
06 6IMIPENEM AND CILASTATIN
07 2IMIPENEM AND CILASTATIN FOR INJECTION USP
08 2IMIPENEM/CILASTATIN 500MG/500MG FRESENIUS
09 1IMIPENEM/CILASTATIN Atb®
10 1IMIPEX
11 1Imcil 500mg**
12 1Imecitin
13 1Imicilast
14 3Imipenem And Cilastatin
15 1Imipenem Cilastatin
16 1Imipenem-Cilastatin Labatec
17 1Imipenem-Cilastatin-Mepha iv
18 2Imipenem/Cilastatin Actavis
19 1Imipenem/Cilastatin Adco 500mg/20ml
20 1Imipenem/Cilastatin Aptapharma
21 1Imipenem/Cilastatin Atb
22 2Imipenem/Cilastatin Elc
23 1Imipenem/Cilastatin Fresenius Kabi
24 1Imipenem/Cilastatin Hospira
25 1Imipenem/Cilastatin Hospira Pdr For Soln
26 2Imipenem/Cilastatin Kabi
27 1Imipenem/Cilastatin Orifarm
28 1Imipenem/Cilastatin Pfizer
29 1Imipenem/Cilastatin Ranbaxy
30 2Imipenem/Cilastatin Sandoz
31 1Imipenem/Cilastatin Steriscience
32 1Imipenem/Cilastatin Stravencon
33 1Imipenem/Cilastatin Teva
34 1Imipenem/Cilastatina Aurovitas
35 2Imipenem; Cilastatin
36 4Imipenem;Cilastatin
37 1Miron
38 6PRIMAXIN
39 2Primaxin Iv
40 1RECARBRIO
41 1Recarbrio
42 1Sepencil 500 mg
43 2TARO-IMIPENEM-CILASTATIN
44 1TIASEP
45 5Tienam
46 1Tienam 500
47 1Tipem
48 8Blank
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01 4Canada
02 1France
03 1Georgia
04 13India
05 6Italy
06 6Malta
07 4Norway
08 1Romania
09 10South Africa
10 2South Korea
11 5Spain
12 15Sweden
13 2Switzerland
14 13USA
Regulatory Info :
Registration Country : India
Brand Name : Imipenem; Cilastatin
Dosage Form : Sterile Vial
Dosage Strength : 250MG; 250
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Imipenem; Cilastatin
Dosage Form : Sterile Vial
Dosage Strength : 500MG; 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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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

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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

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Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 250MG; 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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
