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01 2ABRAXIS PHARM

02 4Abbott Laboratories

03 4Amphastar Pharmaceuticals

04 8Baxter Healthcare Corporation

05 3Bristol Laboratories Ltd

06 6Eli Lilly

07 2Eurocept International B.V .

08 3GSK

09 1Hainan Haiyao

10 2Villerton Invest Said

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1985-09-11

Application Number : 62547

Regulatory Info : DISCN

Registration Country : USA

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1985-09-11

Application Number : 62547

Regulatory Info : DISCN

Registration Country : USA

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1985-09-11

Application Number : 62548

Regulatory Info : DISCN

Registration Country : USA

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1985-09-11

Application Number : 62548

Regulatory Info : DISCN

Registration Country : USA

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1987-06-10

Application Number : 62666

Regulatory Info : DISCN

Registration Country : USA

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1987-06-10

Application Number : 62666

Regulatory Info : DISCN

Registration Country : USA

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 1985-05-03

Application Number : 62426

Regulatory Info : DISCN

Registration Country : USA

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1985-05-03

Application Number : 62426

Regulatory Info : DISCN

Registration Country : USA

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1985-05-03

Application Number : 62426

Regulatory Info : DISCN

Registration Country : USA

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4GM BASE/VIAL

Packaging :

Approval Date : 1985-05-03

Application Number : 62426

Regulatory Info : DISCN

Registration Country : USA

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11

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 1984-01-31

Application Number : 62422

Regulatory Info : DISCN

Registration Country : USA

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12

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1984-01-31

Application Number : 62422

Regulatory Info : DISCN

Registration Country : USA

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13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 1984-01-31

Application Number : 62422

Regulatory Info : DISCN

Registration Country : USA

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14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1984-01-31

Application Number : 62422

Regulatory Info : DISCN

Registration Country : USA

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15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 1991-07-16

Application Number : 62422

Regulatory Info : DISCN

Registration Country : USA

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16

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1991-07-16

Application Number : 62422

Regulatory Info : DISCN

Registration Country : USA

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17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20MG BASE/ML

Packaging :

Approval Date : 1987-03-05

Application Number : 62730

Regulatory Info : DISCN

Registration Country : USA

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18

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML

Packaging :

Approval Date : 1987-03-05

Application Number : 62730

Regulatory Info : DISCN

Registration Country : USA

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19

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1984-05-07

Application Number : 62464

Regulatory Info : DISCN

Registration Country : USA

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20

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1984-05-07

Application Number : 62464

Regulatory Info : DISCN

Registration Country : USA

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21

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : CEPHALOTHIN SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4GM BASE/VIAL

Packaging :

Approval Date : 1984-05-07

Application Number : 62464

Regulatory Info : DISCN

Registration Country : USA

blank

22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : KEFLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 50482

Regulatory Info : DISCN

Registration Country : USA

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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : KEFLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 50482

Regulatory Info : DISCN

Registration Country : USA

blank

24

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : KEFLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4GM BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 50482

Regulatory Info : DISCN

Registration Country : USA

blank

25

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : KEFLIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 20GM BASE/VIAL

Packaging :

Approval Date : 1982-01-01

Application Number : 50482

Regulatory Info : DISCN

Registration Country : USA

blank

26

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : KEFLIN IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1985-09-10

Application Number : 62549

Regulatory Info : DISCN

Registration Country : USA

blank

27

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : KEFLIN IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1985-09-10

Application Number : 62549

Regulatory Info : DISCN

Registration Country : USA

blank

28

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : SEFFIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 1983-11-15

Application Number : 62435

Regulatory Info : DISCN

Registration Country : USA

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29

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : SEFFIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 1983-11-15

Application Number : 62435

Regulatory Info : DISCN

Registration Country : USA

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30

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CEPHALOTHIN SODIUM

Brand Name : SEFFIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 10GM BASE/VIAL

Packaging :

Approval Date : 1983-11-15

Application Number : 62435

Regulatory Info : DISCN

Registration Country : USA

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