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 1HQ SPCLT PHARMA
16 2Hanlim Pharmaceuticals Inc
17 14Hikma Pharmaceuticals
18 5Hospira, Inc.
19 1MIP Pharma
20 6Orofino Pharmaceuticals Group
21 4QILU ANTIBIOTICS
22 1Reyoung pharmaceutical
23 3STERIMAX INC
24 2Samson Medical Technologies
25 7Sandoz B2B
26 2Steri-Pharma LLC
27 8Teva Pharmaceutical Industries
28 3Umedica Laboratories
01 1Dry Powder Injectable
02 87INJECTABLE;INJECTION
03 5INJECTION
04 1POWDER FOR INJECTION / INFUSION
05 15POWDER FOR SOLUTION
06 3POWDER;INTRAVENOUS
07 7Powder for Injection
08 1Powder for injection
09 1SOLUTION
10 3SOLUTION;INTRAVENOUS
01 67DISCN
02 5Generic
03 16Prescription
04 26RX
05 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 INJECTION, USP
11 68CEFAZOLIN SODIUM
12 3CEFAZOLIN SODIUM FOR INJECTION BP
13 1Cefazolin MIP
14 1Cefazoline Sodium
15 2HANLIM CEFAZOLIN SODIUM
16 7KEFZOL
17 3UZOLINE
18 8Blank
01 16Canada
02 1China
03 4India
04 6Italy
05 2South Korea
06 1Sweden
07 93USA
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 : 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
