01 8ALKEM LABS LTD
02 2ANDA REPOSITORY
03 8APOTHECON
04 3AUROBINDO PHARMA
05 2AUROBINDO PHARMA LTD
06 6BARR
07 2BELCHER PHARMS
08 4CHARTWELL RX
09 5FACTA FARMA
10 2HIKMA
11 2HIKMA PHARMS
12 2IVAX SUB TEVA PHARMS
13 5LILLY
14 4LUPIN
15 7PRAGMA
16 2PUREPAC PHARM
17 2RANBAXY LABS LTD
18 2STEVENS J
19 2SUN PHARM INDS (IN)
20 4SUN PHARM INDS LTD
21 14TEVA
22 5VITARINE
23 2YOSHITOMI
24 2YUNG SHIN PHARM
01 49CAPSULE;ORAL
02 30FOR SUSPENSION;ORAL
03 2TABLET, FOR SUSPENSION;ORAL
04 16TABLET;ORAL
01 66DISCN
02 31RX
01 83CEPHALEXIN
02 5KEFLET
03 7KEFLEX
04 2PANIXINE DISPERDOSE
01 88No
02 9Yes
RLD : Yes
TE Code :
Brand Name : KEFLET
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1982-01-01
Application Number : 50440
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : KEFLET
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1GM BASE
Approval Date : 1982-01-01
Application Number : 50440
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : KEFLET
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 1987-02-26
Application Number : 50440
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 333MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2006-05-12
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 750MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2006-05-12
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1982-01-01
Application Number : 50406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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*
Approval Date : 1982-01-01
Application Number : 50406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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*
Approval Date : 1982-01-01
Application Number : 50406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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