01 3APOTEX INC
02 3AUROBINDO PHARMA LTD
03 2AVET LIFESCIENCES
04 4BAXTER HLTHCARE CORP
05 1BEDFORD LABS
06 3CHARTWELL MOLECULAR
07 3CHARTWELL RX
08 3DR REDDYS LABS INC
09 5EUGIA PHARMA
10 3FRESENIUS KABI USA
11 5GLAND
12 3GLENMARK PHARMS LTD
13 3HEC PHARM
14 3HETERO LABS LTD V
15 3HIKMA FARMACEUTICA
16 3HIKMA PHARMS
17 5HOSPIRA
18 3INFORLIFE
19 9JANSSEN PHARMS
20 2JUBILANT GENERICS
21 3KNACK
22 1LANNETT CO INC
23 3LUPIN
24 3MACLEODS PHARMS LTD
25 1MICRO LABS LTD INDIA
26 3MYLAN PHARMA
27 3NATCO PHARMA
28 1NOVITIUM PHARMA
29 3ORBION PHARMS
30 3PHARMOBEDIENT
31 3RISING
32 1RUBICON RESEARCH
33 3SANDOZ
34 2SANTEN
35 1SCIEGEN PHARMS
36 1SICOR PHARMS
37 3TEVA
38 3TORRENT PHARMS
39 3WATSON LABS INC
40 1WATSON LABS TEVA
41 3ZYDUS LIFESCIENCES
42 2ZYDUS PHARMS
01 2INJECTABLE; INJECTION
02 44INJECTABLE;INJECTION
03 8SOLUTION/DROPS;OPHTHALMIC
04 3SOLUTION;ORAL
05 6TABLET; ORAL
06 56TABLET;ORAL
01 54DISCN
02 57RX
03 8Blank
01 1IQUIX
02 6LEVAQUIN
03 3LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER
04 83LEVOFLOXACIN
05 24LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
06 1LEVOFLOXACIN; DEXTROSE
07 1QUIXIN
01 100No
02 11Yes
03 8Blank
RLD : Yes
TE Code :
Brand Name : LEVAQUIN
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20634
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20634
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN
Dosage Form : TABLET;ORAL
Dosage Strength : 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2000-09-08
Application Number : 20634
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG/20ML (EQ 25MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20635
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG/50ML (EQ 5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20635
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG/100ML (EQ 5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20635
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 750MG/30ML (EQ 25MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20635
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEVAQUIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 750MG/150ML (EQ 5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-12-20
Application Number : 20635
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : QUIXIN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2000-08-18
Application Number : 21199
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : IQUIX
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2004-03-01
Application Number : 21571
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
