DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 6Dr. Reddy's Laboratories
02 4ABRAXIS PHARM
03 13ACS DOBFAR SPA
04 1Ananta Medicare
05 2Aurobindo Pharma Limited
06 3B. Braun Medical
07 5BEDFORD LABS
08 10Baxter Healthcare Corporation
09 4CEPHAZONE PHARMA
10 2Eli Lilly
11 3Fresenius Kabi Austria
12 4Fresenius Kabi USA
13 6GSK
14 1HQ SPCLT PHARMA
15 2Hanlim Pharmaceuticals Inc
16 14Hikma Pharmaceuticals
17 5Hospira, Inc.
18 1MIP Pharma
19 6Orofino Pharmaceuticals Group
20 4Qilu Pharmaceutical
21 1Reyoung pharmaceutical
22 3STERIMAX INC
23 2Samson Medical Technologies
24 7Sandoz B2B
25 2Steri-Pharma LLC
26 8Teva Pharmaceutical Industries
27 3Umedica Laboratories
01 86INJECTABLE;INJECTION
02 5INJECTION
03 1POWDER FOR INJECTION / INFUSION
04 15POWDER FOR SOLUTION
05 3POWDER;INTRAVENOUS
06 7Powder for Injection
07 1Powder for injection
08 1SOLUTION
09 3SOLUTION;INTRAVENOUS
01 67DISCN
02 5Generic
03 16Prescription
04 25RX
05 9Blank
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 3CEFAZOLIN AND DEXTROSE
06 6CEFAZOLIN FOR INJECTION
07 3CEFAZOLIN FOR INJECTION USP
08 3CEFAZOLIN FOR INJECTION, USP
09 3CEFAZOLIN IN DEXTROSE
10 1CEFAZOLIN INJECTION, USP
11 68CEFAZOLIN SODIUM
12 3CEFAZOLIN SODIUM FOR INJECTION BP
13 1Cefazolin MIP
14 2HANLIM CEFAZOLIN SODIUM
15 7KEFZOL
16 3UZOLINE
17 8Blank
01 16Canada
02 1China
03 3India
04 6Italy
05 2South Korea
06 1Sweden
07 92USA
08 1United Kingdom
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
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFZOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61773
Regulatory Info : DISCN
Registration Country : USA
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
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
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
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
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
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
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
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
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
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
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
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
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