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01 2ANI Pharmaceuticals Inc

02 6Actavis Inc

03 2Antibiotice SA

04 3Aurobindo Pharma Limited

05 2Baxter Healthcare Corporation

06 10Bristol Myers Squibb

07 6ELKINS SINN

08 3Fresenius Kabi USA

09 12GSK

10 2Hospira, Inc.

11 5Istituto Biochimico Italiano Giovanni Lorenzini SpA

12 3Piramal Enterprises Limited

13 2Reyoung pharmaceutical

14 2STERISCIENCE SPECLTS

15 3Sagent Pharmaceuticals

16 7Sandoz B2B

17 1Teva Pharmaceutical Industries

18 3Wockhardt

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PharmaCompass

01

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 1989-10-26

Application Number : 50640

Regulatory Info : RX

Registration Country : USA

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02

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1989-10-26

Application Number : 50640

Regulatory Info : RX

Registration Country : USA

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03

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : PROSTAPHLIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 50118

Regulatory Info : DISCN

Registration Country : USA

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04

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : PROSTAPHLIN

Dosage Form : FOR SOLUTION;ORAL

Dosage Strength : EQ 250MG BASE/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 50194

Regulatory Info : DISCN

Registration Country : USA

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05

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

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 : 50195

Regulatory Info : DISCN

Registration Country : USA

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06

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

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 : 50195

Regulatory Info : DISCN

Registration Country : USA

blank

07

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

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 : 50195

Regulatory Info : DISCN

Registration Country : USA

blank

08

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

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 : 50195

Regulatory Info : DISCN

Registration Country : USA

blank

09

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

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 : 50195

Regulatory Info : DISCN

Registration Country : USA

blank

10

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 61450

Regulatory Info : DISCN

Registration Country : USA

blank

11

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 61450

Regulatory Info : DISCN

Registration Country : USA

blank

12

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

Dosage Form : FOR SOLUTION;ORAL

Dosage Strength : EQ 250MG BASE/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 61457

Regulatory Info : DISCN

Registration Country : USA

blank

13

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

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 : 1982-03-26

Application Number : 61334

Regulatory Info : DISCN

Registration Country : USA

blank

14

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

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 : 1982-03-26

Application Number : 61334

Regulatory Info : DISCN

Registration Country : USA

blank

15

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

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 : 1982-03-26

Application Number : 61334

Regulatory Info : DISCN

Registration Country : USA

blank

16

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

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 : 1982-03-26

Application Number : 61334

Regulatory Info : DISCN

Registration Country : USA

blank

17

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10GM 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 : 61334

Regulatory Info : DISCN

Registration Country : USA

blank

18

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 250MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 61336

Regulatory Info : DISCN

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : BACTOCILL

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 500MG BASE

Packaging :

Approval Date : 1982-01-01

Application Number : 61336

Regulatory Info : DISCN

Registration Country : USA

blank

20

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

OXACILLIN SODIUM

Brand Name : OXACILLIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 61490

Regulatory Info : DISCN

Registration Country : USA

blank