DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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01 1Dry Powder Injectable
02 87INJECTABLE;INJECTION
03 5INJECTION
04 1Injectable
05 1Injection
06 1Injection/Infusion Solution
07 15POWDER FOR SOLUTION
08 4POWDER;INTRAVENOUS
09 1Powder And Solvent For Injectable Solution
10 1Powder And Solvent For Intramuscular Injection Solution
11 1Powder And Solvent For Intravenous Injection Solution
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14 1Powder For Intravenous Injection Solution
15 7Powder for Injection
16 1SOLUTION
17 3SOLUTION;INTRAVENOUS
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01 10Authorized
02 1Cancelled
03 68DISCN
04 5Generic
05 17Prescription
06 25RX
07 10Blank
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01 5ANCEF
02 2ANCEF IN DEXTROSE 5% IN PLASTIC CONTAINER
03 2ANCEF IN PLASTIC CONTAINER
04 2ANCEF IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
05 4CEFAZOLIN AND DEXTROSE
06 6CEFAZOLIN FOR INJECTION
07 3CEFAZOLIN FOR INJECTION USP
08 3CEFAZOLIN FOR INJECTION, USP
09 3CEFAZOLIN IN DEXTROSE
10 1CEFAZOLIN IN DEXTROSE INJECTION, USP
11 69CEFAZOLIN SODIUM
12 3CEFAZOLIN SODIUM FOR INJECTION BP
13 1Cefazolin "Mip"
14 1Cefazolin sodium
15 2Cefazolina Ldp Laboratorios Torlan
16 3Cefazolina Normon
17 2Cefazolina Qilu
18 3Cefazolina Sala
19 1Cefazoline Sodium
20 2HANLIM CEFAZOLIN SODIUM
21 7KEFZOL
22 1Tecfazolina
23 3UZOLINE
24 7Blank
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01 16Canada
02 1China
03 1Denmark
04 5India
05 6Italy
06 2South Korea
07 11Spain
08 94USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 1989-12-29
Application Number : 62988
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1989-12-29
Application Number : 62988
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1989-12-29
Application Number : 62988
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5GM BASE/VIAL
Packaging :
Approval Date : 1989-12-29
Application Number : 62989
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL
Packaging :
Approval Date : 1989-12-29
Application Number : 62989
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20GM BASE/VIAL
Packaging :
Approval Date : 1989-12-29
Application Number : 62989
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFZOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61773
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFAZOLIN AND DEXTROSE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2000-07-27
Application Number : 50779
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : CEFAZOLIN AND DEXTROSE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2000-07-27
Application Number : 50779
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : CEFAZOLIN AND DEXTROSE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 2012-01-13
Application Number : 50779
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : CEFAZOLIN AND DEXTROSE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 3GM BASE/VIAL
Packaging :
Approval Date : 2024-08-26
Application Number : 50779
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 1983-06-08
Application Number : 50566
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Packaging :
Approval Date : 1983-06-08
Application Number : 50566
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 1983-06-08
Application Number : 50566
Regulatory Info : DISCN
Registration Country : USA

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Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Packaging :
Approval Date : 1983-06-08
Application Number : 50566
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF
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 : 50461
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF
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 : 50461
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF
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 : 50461
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5GM 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 : 50461
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ANCEF
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 : 50461
Regulatory Info : DISCN
Registration Country : USA
