Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1Xellia Pharmaceuticals ApS

02 2Sanofi

03 1ALTANA

04 1APOTHEKERNES

05 1Antibiotice

06 8Bausch & Lomb Incorporated

07 1Bausch Health

08 3COMBE

09 2DELCOR ASSET

10 1Eli Lilly

11 1Exzell Pharma

12 1Flagship Biotech International Pvt. Ltd

13 1Fulton Medicinali S.p.A

14 1GSK

15 1Huvepharma

16 2Johnson & Johnson

17 4KENVUE CANADA INC.

18 1Lex Ano Uab

19 1Maxfarma, Sa

20 3NASKA

21 1ODAN LABORATORIES LTD

22 4Padagis

23 1Pendopharm

24 1Perrigo Company plc

25 4Pfizer Inc

26 1Pharmaceutical Laboratory Sit - Hygienic Therapeutic Specialties Srl

27 2Pharmaderm

28 2Pharmascience Inc.

29 2Quad Pharma

30 1Reig Jofre

31 3SCIEGEN PHARMS

32 1STERIMAX INC

33 1Safetec

34 3Sandoz B2B

35 1Steri-Med Pharma

36 1TEOFARMA Srl

37 4Taro Pharmaceutical Industries

38 1Teofarma

39 3Teva Pharmaceutical Industries

40 1Vega Biotech Pvt. Ltd.

41 2XGen Pharmaceuticals

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Bacitracin

Brand Name :

Dosage Form : Injection

Dosage Strength : 50000Unit/Vial

Packaging : 1 vial/pack, 10 vials/pack

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : Denmark

Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Bacitracin; Framycetin

Brand Name : Bimixin

Dosage Form :

Dosage Strength : 16 Cpr 2,500 Iu + 25,000 Iu  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Italy

Bacitracin; Framycetin

Brand Name : Bimixin

Dosage Form :

Dosage Strength : The Scir 60 Ml 15,000 Iu + 150,000 Iu  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Sanofi Company Banner

04

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 60731

Regulatory Info : DISCN

Registration Country : USA

blank

05

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : NEO-POLYCIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 60647

Regulatory Info : DISCN

Registration Country : USA

blank

06

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 50416

Regulatory Info : DISCN

Registration Country : USA

blank

07

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : LUMI-SPORYN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 50417

Regulatory Info : RX

Registration Country : USA

blank

08

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN

Brand Name : BACITRACIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 60687

Regulatory Info : DISCN

Registration Country : USA

blank

09

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; POLYMYXIN B SULFATE

Brand Name : POLYSPORIN

Dosage Form : AEROSOL;TOPICAL

Dosage Strength : 10,000 UNITS/GM;2,000,000 UNITS/GM

Packaging :

Approval Date : 1985-03-01

Application Number : 50167

Regulatory Info : DISCN

Registration Country : USA

blank

10

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 60764

Regulatory Info : DISCN

Registration Country : USA

blank

11

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN

Brand Name : BACITRACIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 61212

Regulatory Info : DISCN

Registration Country : USA

blank

12

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : CORTISPORIN

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1984-05-04

Application Number : 50168

Regulatory Info : DISCN

Registration Country : USA

blank

13

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN

Brand Name : BACIGUENT

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 60734

Regulatory Info : DISCN

Registration Country : USA

blank

14

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Brand Name : MYCITRACIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 61048

Regulatory Info : DISCN

Registration Country : USA

blank

15

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC; POLYMYXIN B SULFATE

Brand Name : POLYSPORIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 61229

Regulatory Info : DISCN

Registration Country : USA

blank

16

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN

Brand Name : BACITRACIN

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 500 UNITS/GM

Packaging :

Approval Date : 1982-01-01

Application Number : 62158

Regulatory Info : DISCN

Registration Country : USA

blank

17

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN

Brand Name : BACI-RX

Dosage Form : POWDER;FOR RX COMPOUNDING

Dosage Strength : 5,000,000 UNITS/BOT

Packaging :

Approval Date : 1982-01-01

Application Number : 61580

Regulatory Info : DISCN

Registration Country : USA

blank

18

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

BACITRACIN ZINC

Brand Name : ZIBA-RX

Dosage Form : POWDER;FOR RX COMPOUNDING

Dosage Strength : 500,000 UNITS/BOT

Packaging :

Approval Date : 1982-01-01

Application Number : 61737

Regulatory Info : DISCN

Registration Country : USA

blank

19

COMBE

Country
RDD
Not Confirmed
arrow

COMBE

Country
arrow
RDD
Not Confirmed

BACITRACIN; POLYMYXIN B SULFATE

Brand Name : LANABIOTIC

Dosage Form : DISC;TOPICAL

Dosage Strength : 500 UNITS/GM;5,000 UNITS/GM

Packaging :

Approval Date : 1986-09-22

Application Number : 50598

Regulatory Info : DISCN

Registration Country : USA

blank

20

APOTHEKERNES

Country
RDD
Not Confirmed
arrow

APOTHEKERNES

Country
arrow
RDD
Not Confirmed

BACITRACIN

Brand Name : BACITRACIN

Dosage Form : POWDER;FOR RX COMPOUNDING

Dosage Strength : 5,000,000 UNITS/BOT

Packaging :

Approval Date : 1982-01-01

Application Number : 61699

Regulatory Info : DISCN

Registration Country : USA

blank