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 1Associated Biotech
06 2Aurobindo Pharma Limited
07 4B. Braun Medical
08 5BEDFORD LABS
09 10Baxter Healthcare Corporation
10 4CEPHAZONE PHARMA
11 2Eli Lilly
12 3Fresenius Kabi Austria
13 4Fresenius Kabi USA
14 6GSK
15 2HQ SPCLT PHARMA
16 2Hanlim Pharmaceuticals Inc
17 14Hikma Pharmaceuticals
18 5Hospira, Inc.
19 3LABORATORIOS NORMON SA
20 2Ldp Torlan Laboratories Sa
21 6Orofino Pharmaceuticals Group
22 4Qilu Antibiotics Pharmaceutical Co., Ltd.
23 2Qilu Pharmaceutical
24 3Reig Jofre
25 1Reyoung pharmaceutical
26 3STERIMAX INC
27 2Samson Medical Technologies
28 7Sandoz B2B
29 2Steri-Pharma LLC
30 8Teva Pharmaceutical Industries
31 3Umedica Laboratories
32 1Viamedica, Sl
01 1Dry Powder Injectable
02 87INJECTABLE;INJECTION
03 5INJECTION
04 1Injectable
05 1Injection
06 15POWDER FOR SOLUTION
07 4POWDER;INTRAVENOUS
08 1Powder And Solvent For Injectable Solution
09 1Powder And Solvent For Intramuscular Injection Solution
10 1Powder And Solvent For Intravenous Injection Solution
11 2Powder For Injectable Solution
12 4Powder For Injection And Infusion Solution
13 1Powder For Intravenous Injection Solution
14 7Powder for Injection
15 1SOLUTION
16 3SOLUTION;INTRAVENOUS
01 10Authorized
02 1Cancelled
03 67DISCN
04 5Generic
05 16Prescription
06 26RX
07 10Blank
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 sodium
14 2Cefazolina Ldp Laboratorios Torlan
15 3Cefazolina Normon
16 2Cefazolina Qilu
17 3Cefazolina Sala
18 1Cefazoline Sodium
19 2HANLIM CEFAZOLIN SODIUM
20 7KEFZOL
21 1Tecfazolina
22 3UZOLINE
23 7Blank
01 16Canada
02 1China
03 5India
04 6Italy
05 2South Korea
06 11Spain
07 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
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 : 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 : 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
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
