01 12ACS DOBFAR SPA
02 2ANDA Repository
03 2ANHUI ANKE BIOTECHNOLOGY (GROUP) CO., LTD
04 2Ajanta Pharma Limited
05 8Alkem Laboratories
06 4Associated Biotech
07 5Aurobindo Pharma Limited
08 6Barr Laboratories
09 2Bernofarm Pharmaceutical Company
10 8Bristol Myers Squibb
11 1Brix Biopharma
12 3CRINOS SpA
13 1Central Procurement & Supplies Unit
14 4Chartwell Pharmaceuticals llc
15 6DEVATS INDIA
16 5Eli Lilly
17 1Eloge
18 1Farmarosib SRL
19 2Gulf Drug Company
20 1Hainan Haiyao
21 4Hikma Pharmaceuticals
22 2Hiral Labs
23 2IFA SA Laboratories
24 1IMAEC
25 2IVAX Pharmaceuticals Inc
26 1JMW
27 2Jerome Stevens Pharmaceuticals
28 1Kniss Laboratories
29 1Ldp Torlan Laboratories Sa
30 4Lupin Ltd
31 1MEDOCHEMIE LTD
32 2Meda Ab
33 1Medicem
34 1Medipol Pharmaceutical
35 1National Pharma
36 8Nectar Lifesciences
37 1NeoFarma Pharmaceuticals Limited
38 1Nile Pharma
39 1P & D Pharmaceuticals Limited
40 7PRAGMA PHARMS LLC
41 2PUREPAC PHARM
42 1PVS Laboratories
43 1Phadisco Limited
44 6Pharmascience Inc.
45 4Qualite Pharma
46 1Scott-Edil Pharmacia
47 1Smith & Kenner Pharmaceuticals
48 8Sun Pharmaceutical Industries Limited
49 1TEOFARMA Srl
50 14Teva Pharmaceutical Industries
51 3Umedica Laboratories
52 2Unosource Pharma
53 5VITARINE
54 1Viatris
55 2XL Laboratories Private Limited
56 2Xepa-Soul Pattinson m SDN BHD
57 2YOSHITOMI
58 2Yung Shin Pharm Industrial
59 3Zeiss Pharma
01 1CAP
02 8CAPSULE
03 49CAPSULE;ORAL
04 16Capsule
05 2Capsules
06 1Caspule
07 2Cephalexin 1.000Mg 8 Joined' Oral Use
08 1Cephalexin 5% 100Ml Oral Use
09 1Cephalexin 500Mg 8 Joined' Oral Use
10 1DRY SYRUP
11 4Dispersible Tablet
12 1Dry Powder for Oral Suspension
13 2Dry Syrup
14 1FCT
15 30FOR SUSPENSION;ORAL
16 3Film Coated Tablet
17 3Granule For Oral Suspension
18 3Hard Gelatin Capsule
19 1ORAL SUSPENSION
20 1Oral Powder for Reconstitution
21 2Oral Suspension
22 1POWDER FOR SUSPENSION
23 1Powder
24 3SUSPENSION
25 2Suspensions
26 6TABLET
27 2TABLET, FOR SUSPENSION;ORAL
28 16TABLET;ORAL
29 14Tablet
30 3Tablets
01 5Authorised
02 1Cancelled
03 66DISCN
04 3Deregistered
05 17Generic
06 6Prescription
07 31RX
08 2Withdrawn
09 50Blank
01 1Belex 250
02 1Belex 500
03 2CEFABIOTIC
04 83CEPHALEXIN
05 1Cefalexin Mylan
06 1Cefalexin Oral
07 1Cefalexina Arena
08 8Cephalexin
09 1Cepine
10 1Ceporex
11 1Franlex
12 2HALOCEF
13 5KEFLET
14 9KEFLEX
15 6Keflex
16 3Keforal
17 1Medolexin
18 1Neocef 500 mg
19 1Nexporin-125 DT
20 1Niscef
21 2PANIXINE DISPERDOSE
22 1PMS-CEPHALEXIN - TAB 250MG
23 1PMS-CEPHALEXIN - TAB 500MG
24 1PMS-CEPHALEXIN 125 - SUS 125MG/5ML
25 1PMS-CEPHALEXIN 250 - SUS 250MG/5ML
26 1Sofilex
27 1Sofilex OS
28 1Torlasporin Capsules
29 3UCEPH
30 39Blank
01 2Bolivia
02 2Cambodia
03 6Canada
04 3China
05 1Egypt
06 41India
07 11Italy
08 2Malaysia
09 7Malta
10 2South Africa
11 1Spain
12 3Sweden
13 97USA
14 1Venezuela
15 1Vietnam
16 1Blank
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
Packaging :
Approval Date : 1982-01-01
Application Number : 62117
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
Packaging :
Approval Date : 1982-01-01
Application Number : 62117
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
Packaging :
Approval Date : 1982-01-01
Application Number : 62117
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62118
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 62118
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLET
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50440
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLET
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50440
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLET
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1987-02-26
Application Number : 50440
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61969
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61969
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50405
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50405
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 333MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2006-05-12
Application Number : 50405
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 750MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2006-05-12
Application Number : 50405
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50406
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
Packaging :
Approval Date : 1982-01-01
Application Number : 50406
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KEFLEX
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
Packaging :
Approval Date : 1982-01-01
Application Number : 50406
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1987-02-13
Application Number : 62702
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1987-02-13
Application Number : 62702
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CEPHALEXIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 125MG BASE/5ML
Packaging :
Approval Date : 1987-02-13
Application Number : 62703
Regulatory Info : RX
Registration Country : USA
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