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 6Actavis Inc
04 2Amphastar Pharmaceuticals
05 11Antibiotice SA
06 6Associated Biotech
07 4Auro Pharma Inc
08 11Aurobindo Pharma Limited
09 1Aurogen South Africa (Pty) Ltd
10 2Bosch Pharmaceuticals
11 5Bristol Laboratories Ltd
12 5Bristol Myers Squibb
13 5CONSOLIDATED PHARM
14 1Cathay Drug Company
15 3EUGIA PHARMA INC.
16 3Eli Lilly
17 5Flagship Biotech International Pvt. Ltd
18 4Fresenius Kabi Austria
19 8GSK
20 1HANFORD GC
21 12HQ SPECLT PHARMA
22 9Hikma Pharmaceuticals
23 10Hospira, Inc.
24 9Istituto Biochimico Italiano Giovanni Lorenzini SpA
25 2MEDIMETRIKS PHARMS
26 2Navesta
27 1NoroBio Pharmaceutical
28 8Orofino Pharmaceuticals Group
29 6Pfizer Inc
30 8STERISCIENCE SPECLTS
31 6Sagent Pharmaceuticals
32 13Sandoz B2B
33 4Teva Pharmaceutical Industries
34 5Umedica Laboratories
35 2Unichem Laboratories Limited
36 6Unichem Pharmaceuticals USA, Inc
37 16Wyeth Pharmaceuticals Inc
38 3XYZ Pharma
39 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 8Powder for Injection
10 2Powder for Solution for Injection
11 2Powder for injection/infusion, solution
12 1Sterile Powder for Injection
13 4powder for injection
14 1powder for injection/Infusion
15 2Blank
01 89DISCN
02 2Dossier Available
03 19Generic
04 15Prescription
05 63RX
06 34Blank
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 8TOTACILLIN-N
24 5UCILLIN
25 6UNASYN
26 24Blank
01 15Canada
02 7China
03 18India
04 8Italy
05 2Norway
06 2Pakistan
07 1Philippines
08 2Poland
09 5Romania
10 7South Africa
11 2Sri Lanka
12 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
