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01 2Abbott Laboratories

02 1Avet Pharmaceuticals

03 2Bosch Pharmaceuticals

04 9Bristol Myers Squibb

05 3Cooper Pharma Limited

06 1Cuckos

07 4Farbe Firma

08 3Flagship Biotech International Pvt. Ltd

09 2Fresenius Kabi USA

10 5Hikma Pharmaceuticals

11 8Hospira, Inc.

12 2IGI Labs, Inc.

13 3Ind Swift Laboratories Limited

14 1Insmed

15 1JAMP PHARMA

16 2JW Pharmaceutical Corporation

17 1Lifespan Biotech

18 1MARCAN PHARMACEUTICALS INC

19 2Meitheal Pharmaceuticals

20 1Montage Laboratories

21 2Nishchem International Pvt. Ltd

22 2ORIFARM GROUP AS

23 1Omega Laboratories Limited

24 1Omnia Pharmaceutical AB

25 1Qilu Pharmaceutical

26 1Safeline Pharmaceuticals

27 3Sagent Pharmaceuticals

28 1Sandoz B2B

29 3Umedica Laboratories

30 1ZOETIS MANUFACTURING ITALIA S.R.L. IT 95121 Catania

31 2Blank

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PharmaCompass

01

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1994-11-30

Application Number : 63265

Regulatory Info : DISCN

Registration Country : USA

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02

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1994-10-31

Application Number : 63266

Regulatory Info : DISCN

Registration Country : USA

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03

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50495

Regulatory Info : DISCN

Registration Country : USA

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04

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG 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 : 50495

Regulatory Info : DISCN

Registration Country : USA

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05

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10MG BASE/ML

Packaging :

Approval Date : 1987-11-30

Application Number : 50618

Regulatory Info : DISCN

Registration Country : USA

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06

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/ML

Packaging :

Approval Date : 1987-11-30

Application Number : 50618

Regulatory Info : DISCN

Registration Country : USA

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07

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 62311

Regulatory Info : DISCN

Registration Country : USA

blank

08

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 62311

Regulatory Info : DISCN

Registration Country : USA

blank

09

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1984-09-20

Application Number : 62562

Regulatory Info : DISCN

Registration Country : USA

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10

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1984-09-20

Application Number : 62562

Regulatory Info : DISCN

Registration Country : USA

blank

11

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1992-05-18

Application Number : 63274

Regulatory Info : DISCN

Registration Country : USA

blank

12

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1992-05-18

Application Number : 63275

Regulatory Info : DISCN

Registration Country : USA

blank

13

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1994-04-11

Application Number : 63313

Regulatory Info : RX

Registration Country : USA

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14

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1994-04-11

Application Number : 63315

Regulatory Info : RX

Registration Country : USA

blank

15

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1994-11-30

Application Number : 63263

Regulatory Info : DISCN

Registration Country : USA

blank

16

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1994-11-30

Application Number : 63264

Regulatory Info : DISCN

Registration Country : USA

blank

17

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 62.5MG BASE/ML

Packaging :

Approval Date : 1994-10-31

Application Number : 63283

Regulatory Info : DISCN

Registration Country : USA

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18

DIA 2025
Not Confirmed
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DIA 2025
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1993-07-30

Application Number : 63350

Regulatory Info : DISCN

Registration Country : USA

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19

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/ML

Packaging :

Approval Date : 1995-12-14

Application Number : 63167

Regulatory Info : DISCN

Registration Country : USA

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20

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

AMIKACIN SULFATE

Brand Name : AMIKACIN SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/ML

Packaging :

Approval Date : 1995-12-14

Application Number : 63169

Regulatory Info : DISCN

Registration Country : USA

blank