01 12ACS DOBFAR SPA
02 2ANDA Repository
03 2ANHUI ANKE BIOTECHNOLOGY (GROUP) CO., LTD
04 2Ajanta Pharma Limited
05 8Alkem Laboratories
06 2Antibiotice
07 4Associated Biotech
08 5Aurobindo Pharma Limited
09 6Barr Laboratories
10 2Bernofarm Pharmaceutical Company
11 8Bristol Myers Squibb
12 1Brix Biopharma
13 3CRINOS SpA
14 1Central Procurement & Supplies Unit
15 4Chartwell Pharmaceuticals llc
16 6DEVATS INDIA
17 5Eli Lilly
18 1Eloge
19 1Farmarosib SRL
20 2Gulf Drug Company
21 1Hainan Haiyao
22 4Hikma Pharmaceuticals
23 2Hiral Labs
24 2IFA SA Laboratories
25 1IMAEC
26 2IVAX Pharmaceuticals Inc
27 1JMW
28 2Jerome Stevens Pharmaceuticals
29 1Kniss Laboratories
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 17Capsule
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 66DISCN
03 3Deregistered
04 17Generic
05 6Prescription
06 31RX
07 2Withdrawn
08 52Blank
01 1Belex 250
02 1Belex 500
03 2CEFABIOTIC
04 83CEPHALEXIN
05 1Cefalexin Mylan
06 1Cefalexin Oral
07 1Cefalexin? Atb® 250 mg
08 1Cefalexin? Atb® 500 mg
09 1Cefalexina Arena
10 8Cephalexin
11 1Cepine
12 1Ceporex
13 1Franlex
14 2HALOCEF
15 5KEFLET
16 9KEFLEX
17 6Keflex
18 3Keforal
19 1Medolexin
20 1Neocef 500 mg
21 1Nexporin-125 DT
22 1Niscef
23 2PANIXINE DISPERDOSE
24 1PMS-CEPHALEXIN - TAB 250MG
25 1PMS-CEPHALEXIN - TAB 500MG
26 1PMS-CEPHALEXIN 125 - SUS 125MG/5ML
27 1PMS-CEPHALEXIN 250 - SUS 250MG/5ML
28 1Sofilex
29 1Sofilex OS
30 3UCEPH
31 39Blank
01 2Bolivia
02 2Cambodia
03 6Canada
04 3China
05 1Egypt
06 41India
07 11Italy
08 2Malaysia
09 7Malta
10 2Moldova
11 2South Africa
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
