01 3AIPING PHARM INC
02 1ALTAIRE PHARMS INC
03 3AMNEAL
04 1AMRING PHARMS
05 2ANI PHARMS
06 3AUROBINDO PHARMA
07 3BARR
08 5BAYER HLTHCARE
09 2BAYER PHARMS
10 3CARLSBAD
11 3CHARTWELL
12 1DEPOMED INC
13 5DR REDDYS LABS LTD
14 1FDC LTD
15 1FOSUN PHARMA
16 3HIKMA
17 3IVAX SUB TEVA PHARMS
18 2LAB SALVAT
19 3NATCO
20 1NEW HEIGHTSRX
21 3NOSTRUM LABS
22 2PH HEALTH
23 3PLIVA
24 1RENOVA PHARMS
25 6RISING
26 1RUBICON RESEARCH
27 3SANDOZ
28 3SUN PHARM INDS LTD
29 3TARO
30 3TEVA
31 1THE J MOLNER
32 3UNIQUE
33 3WATSON LABS
34 1WATSON LABS INC
35 2YILING
01 1OINTMENT;OPHTHALMIC
02 9SOLUTION/DROPS;OPHTHALMIC
03 3SOLUTION/DROPS;OTIC
04 1SUSPENSION/DROPS;OTIC
05 2TABLET, EXTENDED RELEASE; ORAL
06 12TABLET, EXTENDED RELEASE;ORAL
07 59TABLET;ORAL
01 38DISCN
02 47RX
03 2Blank
01 1CETRAXAL
02 2CILOXAN
03 3CIPRO
04 1CIPRO HC
05 4CIPRO XR
06 9CIPROFLOXACIN EXTENDED RELEASE
07 65CIPROFLOXACIN HYDROCHLORIDE
08 1OTOVEL
09 1PROQUIN XR
01 77No
02 8Yes
03 2Blank
RLD : Yes
TE Code : AB
Brand Name : CIPRO
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 1987-10-22
Application Number : 19537
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : CIPRO
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1987-10-22
Application Number : 19537
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : CIPRO
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 750MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1987-10-22
Application Number : 19537
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Brand Name : CIPRO XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 212.6MG;EQ 287.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2002-12-13
Application Number : 21473
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Brand Name : CIPRO XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 425.2MG;EQ 574.9MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2003-08-28
Application Number : 21473
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Brand Name : CIPRO XR
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Dosage Strength : 212.6MG; EQ 287.5MG BASE
Approval Date :
Application Number : 21554
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Brand Name : CIPRO XR
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Dosage Strength : 425.2MG; EQ 574.9MG BASE
Approval Date :
Application Number : 21554
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code : AT
Brand Name : CILOXAN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.3% BASE
Approval Date : 1990-12-31
Application Number : 19992
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT
RLD : Yes
TE Code :
Brand Name : CILOXAN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 0.3% BASE
Approval Date : 1998-03-30
Application Number : 20369
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE
Brand Name : CIPRO HC
Dosage Form : SUSPENSION/DROPS;OTIC
Dosage Strength : EQ 0.2% BASE;1%
Approval Date : 1998-02-10
Application Number : 20805
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
