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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    USP reference standards; highly characterized specimens of drug substances, impurities, excipients, degradation products & more.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Guizhou Utide Biotechnology Co., Ltd. - Specialized GMP manufacturing for next-generation GLP-1 peptide APIs.

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    Cefalotin sodium Sterile

    ACTIVE PHARMA INGREDIENTS

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    Amphastar Pharmaceuticals

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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

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    CEPHALOTHIN SODIUM

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    Approval Date : 1985-05-03

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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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    CEPHALOTHIN SODIUM

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    Baxter Healthcare Corporation

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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

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    Baxter Healthcare Corporation

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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

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    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

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    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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    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 : 1991-07-16

    Application Number : 62422

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    Registration Country : USA

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    Baxter Healthcare Corporation

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    CEPHALOTHIN SODIUM

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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

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    Approval Date : 1991-07-16

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    11

    Bristol Laboratories Ltd

    United Kingdom
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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM 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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    12

    Bristol Laboratories Ltd

    United Kingdom
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    CEPHALOTHIN SODIUM

    Brand Name : CEPHALOTHIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 1984-05-07

    Application Number : 62464

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    13

    Bristol Laboratories Ltd

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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

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    Eli Lilly

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    CEPHALOTHIN SODIUM

    Brand Name : KEFLIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 50482

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    Eli Lilly

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    CEPHALOTHIN SODIUM

    Brand Name : KEFLIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 50482

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    Eli Lilly

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    CEPHALOTHIN SODIUM

    Brand Name : KEFLIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

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    Approval Date : 1982-01-01

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    Eli Lilly

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    CEPHALOTHIN SODIUM

    Brand Name : KEFLIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 50482

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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

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    Approval Date : 1983-11-15

    Application Number : 62435

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    GSK

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    CEPHALOTHIN SODIUM

    Brand Name : SEFFIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 1983-11-15

    Application Number : 62435

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    GSK

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    CEPHALOTHIN SODIUM

    Brand Name : SEFFIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL

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    Approval Date : 1983-11-15

    Application Number : 62435

    Regulatory Info : DISCN

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