Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
01 4Polfa Tarchomin
02 7ACS DOBFAR SPA
03 1ALPHARMA
04 6Actavis Inc
05 2Amphastar Pharmaceuticals
06 11Antibiotice
07 6Associated Biotech
08 4Auro Pharma Inc
09 11Aurobindo Pharma Limited
10 1Aurogen South Africa (Pty) Ltd
11 2Bosch Pharmaceuticals
12 5Bristol Laboratories Ltd
13 5Bristol Myers Squibb
14 5CONSOLIDATED PHARM
15 1Cathay Drug Company
16 3EUGIA PHARMA INC.
17 3Eli Lilly
18 5Flagship Biotech International Pvt. Ltd
19 4Fresenius Kabi Austria
20 8GSK
21 1HANFORD GC
22 12HQ SPECLT PHARMA
23 9Hikma Pharmaceuticals
24 10Hospira, Inc.
25 9Istituto Biochimico Italiano Giovanni Lorenzini SpA
26 2MEDIMETRIKS PHARMS
27 2Navesta
28 1NoroBio Pharmaceutical
29 8ONESOURCE SPECIALTY
30 8Orofino Pharmaceuticals Group
31 6Pfizer Inc
32 6Sagent Pharmaceuticals
33 13Sandoz B2B
34 4Teva Pharmaceutical Industries
35 5Umedica Laboratories
36 2Unichem Laboratories Limited
37 6Unichem Pharmaceuticals USA, Inc
38 16Wyeth Pharmaceuticals Inc
39 3XYZ Pharma
40 6Xiangbei Welman Pharmaceuticals
01 6Dry Powder Injectable
02 2Dry Powder Injection
03 7INJ
04 151INJECTABLE;INJECTION
05 3INJECTION
06 16Injection
07 15POWDER FOR SOLUTION
08 2POWDER;INTRAVENOUS
09 1Powder For Injection
10 8Powder for Injection
11 2Powder for Solution for Injection
12 2Powder for injection/infusion, solution
13 1Sterile Powder for Injection
14 4powder for injection
15 1powder for injection/Infusion
16 2Blank
01 89DISCN
02 2Dossier Available
03 19Generic
04 63RX
05 50Blank
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 2Ampicillin Sodium
12 2Ampicillin;Cloxacillin
13 2Ampin
14 2Ampitar
15 2Ampoxin 1000
16 2Ampoxin 250
17 2Ampoxin 500
18 1Auro Ampicillin Injection 500 mg
19 10OMNIPEN-N
20 6PENBRITIN-S
21 5POLYCILLIN-N
22 1Silgram
23 1Sulmacefta
24 8TOTACILLIN-N
25 5UCILLIN
26 6UNASYN
27 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 2Sri Lanka
13 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
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 : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 1993-12-10
Application Number : 50608
Regulatory Info : RX
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OMNIPEN-N
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 125MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 60626
Regulatory Info : DISCN
Registration Country : USA
