01 7ACS DOBFAR SPA
02 1ALPHARMA
03 6Actavis Inc
04 3Adelco Chromatourgia Athinon E. Colocotronis Bros Sa
05 2Amphastar Pharmaceuticals
06 16Antibiotice
07 2Apta Medica Internacional
08 2Apta Medica Internacional d.o.o
09 2Apta Medica International Doo
10 6Associated Biotech
11 2AstraZeneca
12 4Auro Pharma Inc
13 11Aurobindo Pharma Limited
14 1Aurogen South Africa (Pty) Ltd
15 2Bosch Pharmaceuticals
16 5Bristol Laboratories Ltd
17 5Bristol Myers Squibb
18 5CONSOLIDATED PHARM
19 1Cathay Drug Company
20 2Chemifarma, Sa
21 3Eli Lilly
22 3Eugia Pharma
23 5Flagship Biotech International Pvt. Ltd
24 4Fresenius Kabi Austria
25 8GSK
26 1HANFORD GC
27 12HQ SPECLT PHARMA
28 9Hikma Pharmaceuticals
29 10Hospira, Inc.
30 9Istituto Biochimico Italiano Giovanni Lorenzini SpA
31 3LABORATORIOS NORMON SA
32 2MEDIMETRIKS PHARMS
33 4MEDOCHEMIE LTD
34 2Navesta
35 1NoroBio Pharmaceutical
36 8ONESOURCE SPECIALTY
37 8Orofino Pharmaceuticals Group
38 6Pfizer Inc
39 6Polfa Tarchomin
40 2Reig Jofre
41 1Reiwa Healthcare Sl
42 2SGS Pharma Magyarország Kft.
43 10STADA Arzneimittel
44 6Sagent Pharmaceuticals
45 13Sandoz B2B
46 4Teva Pharmaceutical Industries
47 2Tillomed Laboratories Ltd
48 5Umedica Laboratories
49 2Unichem Laboratories Limited
50 6Unichem Pharmaceuticals USA, Inc
51 1Viatris
52 16Wyeth Pharmaceuticals Inc
53 3XYZ Pharma
54 6Xiangbei Welman Pharmaceuticals
01 6Dry Powder Injectable
02 2Dry Powder Injection
03 7INJ
04 151INJECTABLE;INJECTION
05 3INJECTION
06 3Injectable
07 16Injection
08 27Injection/Infusion Solution
09 15POWDER FOR SOLUTION
10 2POWDER;INTRAVENOUS
11 3Powder For Injection
12 2Powder For Injection And Infusion Solution
13 8Powder For Solution For Injection
14 2Powder For Solution For Injection And Infusion
15 8Powder for Injection
16 2Powder for Solution for Injection
17 1Solution For Injection And Infusion
18 1Sterile Powder for Injection
19 2Suppository
20 4powder for injection
21 1powder for injection/Infusion
22 2Blank
01 9Approved
02 2Authorised
03 8Authorized
04 2Cancelled
05 93DISCN
06 2Deregistered
07 2Dossier Available
08 19Generic
09 5Marketed
10 1Not Marketed
11 33Prescription
12 59RX
13 33Blank
01 4 AMPICILLIN Atb®
02 1 AMPIPLUS®
03 1AMPICIL 1000
04 1AMPICIL 250
05 37AMPICILLIN AND SULBACTAM
06 4AMPICILLIN FOR INJECTION, USP
07 81AMPICILLIN SODIUM
08 7AMPICILLIN SODIUM FOR INJECTION BP
09 4AMPICILLIN SODIUM FOR INJECTION, USP
10 2Amipicillin;Sulbactam
11 2Ampicilina Tillomed
12 1Ampicilina/Sulbactam Reiwa Healthcare
13 2Ampicillin SGS Pharma
14 4Ampicillin STADA
15 2Ampicillin Sodium
16 2Ampicillin Stada Nordic
17 4Ampicillin "Medochemie"
18 2Ampicillin "Stada Nordic"
19 2Ampicillin "Stada"
20 4Ampicillin/Sulbactam Aptapharma
21 2Ampicillin/Sulbactam "Aptapharma"
22 2Ampicillin;Cloxacillin
23 2Ampin
24 4Ampitar
25 2Ampoxin 1000
26 2Ampoxin 250
27 2Ampoxin 500
28 5Amroliv
29 1Auro Ampicillin Injection 500 mg
30 2Britapen
31 3Doktacillin
32 3Gobemicin
33 10OMNIPEN-N
34 6PENBRITIN-S
35 5POLYCILLIN-N
36 1Retarpen
37 1Retarpen Vial
38 3Rotacin
39 1Silgram
40 1Sulmacefta
41 8TOTACILLIN-N
42 5UCILLIN
43 6UNASYN
44 24Blank
01 15Canada
02 7China
03 18Denmark
04 18India
05 8Italy
06 2Malta
07 6Norway
08 2Pakistan
09 1Philippines
10 2Poland
11 5Romania
12 1Russia
13 7South Africa
14 10Spain
15 2Sri Lanka
16 11Sweden
17 153USA
Regulatory Info : Prescription
Registration Country : Canada
AMPICILLIN (AMPICILLIN SODIUM)
Brand Name : AMPICILLIN SODIUM FOR INJECTION BP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500MG/VIAL
Packaging : 10ML
Approval Date :
Application Number : 2462311
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
AMPICILLIN (AMPICILLIN SODIUM)
Brand Name : AMPICILLIN SODIUM FOR INJECTION BP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1G/VIAL
Packaging : 15ML
Approval Date :
Application Number : 2462338
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
AMPICILLIN (AMPICILLIN SODIUM)
Brand Name : AMPICILLIN SODIUM FOR INJECTION BP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2G/VIAL
Packaging : 20ML
Approval Date :
Application Number : 2462346
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
Brand Name : POLYCILLIN-N
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : POLYCILLIN-N
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : POLYCILLIN-N
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : POLYCILLIN-N
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
AMPICILLIN (AMPICILLIN SODIUM)
Brand Name : AMPICILLIN SODIUM FOR INJECTION BP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date :
Application Number : 2530481
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
AMPICILLIN (AMPICILLIN SODIUM)
Brand Name : AMPICILLIN SODIUM FOR INJECTION BP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1G/VIAL
Packaging :
Approval Date :
Application Number : 2530503
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
AMPICILLIN (AMPICILLIN SODIUM)
Brand Name : AMPICILLIN SODIUM FOR INJECTION BP
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2G/VIAL
Packaging :
Approval Date :
Application Number : 2530511
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Ampoxin 250
Dosage Form : INJ
Dosage Strength : 125mg/7.5 ml
Packaging : 7.5X10mg/7.5 ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Ampoxin 250
Dosage Form : INJ
Dosage Strength : 125mg/7.5 ml
Packaging : 7.5X1mg/7.5 ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Ampoxin 500
Dosage Form : INJ
Dosage Strength : 250mg/7.5 ml
Packaging : 7.5X10mg/7.5 ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50072
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50072
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50072
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50072
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50072
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50072
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Auro Ampicillin Injection 500 mg
Dosage Form : INJ
Dosage Strength : 500mg
Packaging : 1X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
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