Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
01 6Polfa Tarchomin
02 7ACS DOBFAR SPA
03 1ALPHARMA
04 6Actavis Inc
05 2Amphastar Pharmaceuticals
06 13Antibiotice
07 2Apta Medica Internacional
08 6Associated Biotech
09 2AstraZeneca
10 4Auro Pharma Inc
11 11Aurobindo Pharma Limited
12 1Aurogen South Africa (Pty) Ltd
13 2Bosch Pharmaceuticals
14 5Bristol Laboratories Ltd
15 5Bristol Myers Squibb
16 5CONSOLIDATED PHARM
17 1Cathay Drug Company
18 3EUGIA PHARMA INC.
19 3Eli Lilly
20 5Flagship Biotech International Pvt. Ltd
21 4Fresenius Kabi Austria
22 8GSK
23 1HANFORD GC
24 12HQ SPECLT PHARMA
25 9Hikma Pharmaceuticals
26 10Hospira, Inc.
27 9Istituto Biochimico Italiano Giovanni Lorenzini SpA
28 3LABORATORIOS NORMON SA
29 2MEDIMETRIKS PHARMS
30 2Navesta
31 1NoroBio Pharmaceutical
32 8ONESOURCE SPECIALTY
33 8Orofino Pharmaceuticals Group
34 6Pfizer Inc
35 2Reig Jofre
36 1Reiwa Healthcare Sl
37 2STADA Arzneimittel
38 6Sagent Pharmaceuticals
39 13Sandoz B2B
40 4Teva Pharmaceutical Industries
41 2Tillomed Laboratories Ltd
42 5Umedica Laboratories
43 2Unichem Laboratories Limited
44 6Unichem Pharmaceuticals USA, Inc
45 1Viatris
46 16Wyeth Pharmaceuticals Inc
47 3XYZ Pharma
48 6Xiangbei Welman Pharmaceuticals
01 6Dry Powder Injectable
02 2Dry Powder Injection
03 7INJ
04 151INJECTABLE;INJECTION
05 3INJECTION
06 3Injectable
07 16Injection
08 9Injection/Infusion Solution
09 15POWDER FOR SOLUTION
10 2POWDER;INTRAVENOUS
11 1Powder For Injection
12 2Powder For Injection And Infusion Solution
13 2Powder For Solution For Injection
14 1Powder For Solution For Injection And Infusion
15 8Powder for Injection
16 2Powder for Solution for Injection
17 2Powder for injection/infusion, solution
18 1Sterile Powder for Injection
19 2Suppository
20 4powder for injection
21 1powder for injection/Infusion
22 2Blank
01 9Approved
02 8Authorized
03 89DISCN
04 2Deregistered
05 2Dossier Available
06 19Generic
07 15Prescription
08 63RX
09 35Blank
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 Sodium
14 2Ampicillin Stada Nordic
15 2Ampicillin/Sulbactam Aptapharma
16 2Ampicillin;Cloxacillin
17 2Ampin
18 4Ampitar
19 2Ampoxin 1000
20 2Ampoxin 250
21 2Ampoxin 500
22 2Amroliv
23 1Auro Ampicillin Injection 500 mg
24 2Britapen
25 3Doktacillin
26 3Gobemicin
27 10OMNIPEN-N
28 6PENBRITIN-S
29 5POLYCILLIN-N
30 1Silgram
31 1Sulmacefta
32 8TOTACILLIN-N
33 5UCILLIN
34 6UNASYN
35 24Blank
01 15Canada
02 7China
03 18India
04 8Italy
05 2Norway
06 2Pakistan
07 1Philippines
08 2Poland
09 5Romania
10 1Russia
11 7South Africa
12 8Spain
13 2Sri Lanka
14 11Sweden
15 153USA
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info : Dossier Available
Registration Country : Poland
Brand Name :
Dosage Form : Powder for Solution for Injection
Dosage Strength : 1000MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Dossier Available
Registration Country : Poland
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info : Dossier Available
Registration Country : Poland
Brand Name :
Dosage Form : Powder for Solution for Injection
Dosage Strength : 2000MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Dossier Available
Registration Country : Poland
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info :
Registration Country : Norway
Brand Name : Ampitar
Dosage Form : Powder for injection/infusion, solution
Dosage Strength : 1 g
Packaging : Vials 10 1g
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info :
Registration Country : Norway
Brand Name : Ampitar
Dosage Form : Powder for injection/infusion, solution
Dosage Strength : 2 g
Packaging : Vials 10 2g
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ampitar
Dosage Form : Injection/Infusion Solution
Dosage Strength : 1g
Packaging :
Approval Date : 19/01/2023
Application Number : 20210825000015
Regulatory Info : Approved
Registration Country : Sweden
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ampitar
Dosage Form : Injection/Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 19/01/2023
Application Number : 20210825000022
Regulatory Info : Approved
Registration Country : Sweden
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 : DISCN
Registration Country : USA
Brand Name : POLYCILLIN-N
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 : 50309
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1986-12-31
Application Number : 50608
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1986-12-31
Application Number : 50608
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL;EQ 250MG BASE/VIAL
Packaging :
Approval Date : 1986-12-31
Application Number : 50608
Regulatory Info : DISCN
Registration Country : USA
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
