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01 1Xellia Pharmaceuticals ApS

02 2Actavis Inc

03 1Aurobindo Pharma Limited

04 2B. Braun Medical

05 1BGP PHARMA ULC

06 1Baxter Healthcare Corporation

07 3Bristol Myers Squibb

08 5Eli Lilly

09 1Epic Pharma. LLC.

10 2Eurocept Pharmaceuticals

11 2Fresenius Kabi Austria

12 4Fresenius Kabi USA

13 4GLAND PHARMA LIMITED

14 1Ha Noi CPC1 Pharmaceutical JSC

15 1Hainan Poly Pharm

16 5Hikma Pharmaceuticals

17 8Hospira, Inc.

18 4IGI Labs, Inc.

19 1JAMP PHARMA

20 1JW Pharmaceutical Corporation

21 2LABORATORIOS NORMON SA

22 2Meracine

23 1Montage Laboratories

24 2ORIFARM GROUP AS

25 2Rajasthan Antibiotics

26 1STERIMAX INC

27 2Sandoz B2B

28 1Slate Run Pharmaceuticals

29 2Teva Pharmaceutical Industries

30 1Umedica Laboratories

31 1Viatris

32 1XGen Pharmaceuticals

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PharmaCompass

01

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.2GM BASE/VIAL

Packaging :

Approval Date : 2014-09-16

Application Number : 205685

Regulatory Info : RX

Registration Country : USA

Company Banner

02

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1989-08-09

Application Number : 62945

Regulatory Info : DISCN

Registration Country : USA

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03

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1989-08-09

Application Number : 62945

Regulatory Info : DISCN

Registration Country : USA

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04

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : NEBCIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 50477

Regulatory Info : DISCN

Registration Country : USA

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05

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : NEBCIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.2GM 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 : 50519

Regulatory Info : DISCN

Registration Country : USA

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06

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : NEBCIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 62008

Regulatory Info : DISCN

Registration Country : USA

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07

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : NEBCIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 62008

Regulatory Info : DISCN

Registration Country : USA

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08

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : NEBCIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1987-04-29

Application Number : 62707

Regulatory Info : DISCN

Registration Country : USA

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09

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.2GM BASE/VIAL

Packaging :

Approval Date : 2004-07-13

Application Number : 50789

Regulatory Info : RX

Registration Country : USA

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10

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1991-04-26

Application Number : 63113

Regulatory Info : DISCN

Registration Country : USA

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11

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1991-04-26

Application Number : 63117

Regulatory Info : RX

Registration Country : USA

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12

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1991-07-29

Application Number : 63118

Regulatory Info : DISCN

Registration Country : USA

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13

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1991-04-30

Application Number : 63080

Regulatory Info : DISCN

Registration Country : USA

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14

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 80MG BASE/100ML

Packaging :

Approval Date : 1990-07-31

Application Number : 63081

Regulatory Info : DISCN

Registration Country : USA

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15

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.2MG BASE/ML

Packaging :

Approval Date : 1990-07-31

Application Number : 63081

Regulatory Info : DISCN

Registration Country : USA

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16

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1.6MG BASE/ML

Packaging :

Approval Date : 1993-06-02

Application Number : 63081

Regulatory Info : DISCN

Registration Country : USA

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17

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1991-04-30

Application Number : 63111

Regulatory Info : RX

Registration Country : USA

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18

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1991-04-30

Application Number : 63112

Regulatory Info : DISCN

Registration Country : USA

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19

RDD
Not Confirmed
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Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE (PHARMACY BULK)

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1992-05-18

Application Number : 63116

Regulatory Info : DISCN

Registration Country : USA

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20

RDD
Not Confirmed
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RDD
Not Confirmed

TOBRAMYCIN SULFATE

Brand Name : TOBRAMYCIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1992-01-30

Application Number : 63100

Regulatory Info : DISCN

Registration Country : USA

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