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

filter clear-filterReset all filters

01 1DR REDDYS LABS SA

02 2MANKIND PHARMA

03 1ALCON PHARMS LTD

04 2ALEMBIC

05 1ALKEM LABS LTD

06 1AMNEAL

07 1AMNEAL PHARMS

08 1APOTEX INC

09 1BAUSCH AND LOMB

10 2BAUSCH AND LOMB INC

11 1CHARTWELL RX

12 1CHIESI

13 1EPIC PHARMA LLC

14 1GLAND

15 2HARROW EYE

16 1HIKMA

17 1LUOXIN AUROVITAS

18 1LUPIN

19 1MICRO LABS

20 3NOVARTIS

21 1PADAGIS US

22 1PHARMOBEDIENT

23 1PULMOFLOW INC

24 2SANDOZ

25 1SOMERSET THERAPS LLC

26 1SUN PHARM

27 2TEVA PHARMS USA

28 2VIATRIS

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

RLD : No

TE Code : AN

TOBRAMYCIN

Brand Name : TOBRAMYCIN

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 300MG/5ML

Approval Date : 2018-07-09

Application Number : 207080

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AN

TOBRAMYCIN

Brand Name : TOBRAMYCIN

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 300MG/5ML

Approval Date : 2023-06-30

Application Number : 214478

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AN

TOBRAMYCIN

Brand Name : TOBRAMYCIN

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 300MG/4ML

Approval Date : 2022-09-22

Application Number : 216725

RX/OTC/DISCN : RX

RLD : No

TE Code : AN

Company Banner

04

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

LOTEPREDNOL ETABONATE; TOBRAMYCIN

Brand Name : ZYLET

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 0.5%;0.3%

Approval Date : 2004-12-14

Application Number : 50804

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

05

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

FLUOROMETHOLONE ACETATE; TOBRAMYCIN

Brand Name : TOBRASONE

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 0.1%;0.3%

Approval Date : 1989-07-21

Application Number : 50628

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

06

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

TOBRAMYCIN

Brand Name : TOBREX

Dosage Form : SOLUTION/DROPS;OPHTHALMIC

Dosage Strength : 0.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 50541

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

TOBRAMYCIN

Brand Name : TOBREX

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 0.3%

Approval Date : 1982-01-01

Application Number : 50555

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

08

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

DEXAMETHASONE; TOBRAMYCIN

Brand Name : TOBRADEX

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 0.1%;0.3%

Approval Date : 1988-09-28

Application Number : 50616

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

09

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

DEXAMETHASONE; TOBRAMYCIN

Brand Name : TOBRADEX

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 0.1%;0.3%

Approval Date : 1988-08-18

Application Number : 50592

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

10

PEGS Boston Summit
Not Confirmed
arrow
arrow
PEGS Boston Summit
Not Confirmed

TOBRAMYCIN

Brand Name : TOBI

Dosage Form : SOLUTION;INHALATION

Dosage Strength : 300MG/5ML

Approval Date : 1997-12-22

Application Number : 50753

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AN

blank