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    Amphastar Pharmaceuticals

    U.S.A
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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1985-05-03

    Application Number : 62426

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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 1985-05-03

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    03

    Amphastar Pharmaceuticals

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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 1985-05-03

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    04

    Amphastar Pharmaceuticals

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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

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    Approval Date : 1985-05-03

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    05

    Baxter Healthcare Corporation

    U.S.A
    India Med Expo
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    CEPHALOTHIN SODIUM

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

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML

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    Approval Date : 1984-01-31

    Application Number : 62422

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Baxter Healthcare Corporation

    U.S.A
    India Med Expo
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    CEPHALOTHIN SODIUM

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

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

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    Approval Date : 1984-01-31

    Application Number : 62422

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Baxter Healthcare Corporation

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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML

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    Approval Date : 1984-01-31

    Application Number : 62422

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Baxter Healthcare Corporation

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    Regulatory Info : DISCN

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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

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    Approval Date : 1984-01-31

    Application Number : 62422

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Baxter Healthcare Corporation

    U.S.A
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    Regulatory Info : DISCN

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    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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    10

    Baxter Healthcare Corporation

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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

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    Approval Date : 1991-07-16

    Application Number : 62422

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Bristol Laboratories Ltd

    United Kingdom
    India Med Expo
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    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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    12

    Bristol Laboratories Ltd

    United Kingdom
    India Med Expo
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    United Kingdom
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    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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    13

    Bristol Laboratories Ltd

    United Kingdom
    India Med Expo
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    United Kingdom
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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

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    Approval Date : 1984-05-07

    Application Number : 62464

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    Registration Country : USA

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    14

    Eli Lilly

    U.S.A
    India Med Expo
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    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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    15

    Eli Lilly

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    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

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    16

    Eli Lilly

    U.S.A
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    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

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    17

    Eli Lilly

    U.S.A
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    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

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    18

    GSK

    United Kingdom
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    GSK

    United Kingdom
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    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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    19

    GSK

    United Kingdom
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    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    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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    20

    GSK

    United Kingdom
    India Med Expo
    Not Confirmed
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    GSK

    United Kingdom
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    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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