01 5BAYER HLTHCARE
02 2BAYER PHARMS
03 3AIPING PHARM INC
04 1ALTAIRE PHARMS INC
05 3AMNEAL
06 1AMRING PHARMS
07 2ANI PHARMS
08 3AUROBINDO PHARMA
09 3BARR
10 3CARLSBAD
11 3CHARTWELL
12 1COSETTE PHARMS NC
13 1DEPOMED INC
14 5DR REDDYS LABS LTD
15 1FDC LTD
16 1FOSUN PHARMA
17 3HIKMA
18 3IVAX SUB TEVA PHARMS
19 2LAB SALVAT
20 3NATCO
21 1NEW HEIGHTSRX
22 3NOSTRUM LABS
23 2PH HEALTH
24 1PHARMOBEDIENT
25 3PLIVA
26 6RISING
27 1RUBICON RESEARCH
28 3SANDOZ
29 3SUN PHARM INDS LTD
30 3TARO
31 3TEVA
32 1THE J MOLNER
33 3UNIQUE
34 3WATSON LABS
35 1WATSON LABS INC
36 2YILING
01 1OINTMENT;OPHTHALMIC
02 9SOLUTION/DROPS;OPHTHALMIC
03 3SOLUTION/DROPS;OTIC
04 2SUSPENSION/DROPS;OTIC
05 2TABLET, EXTENDED RELEASE; ORAL
06 12TABLET, EXTENDED RELEASE;ORAL
07 59TABLET;ORAL
01 41DISCN
02 45RX
03 2Blank
01 1CETRAXAL
02 2CILOXAN
03 3CIPRO
04 1CIPRO HC
05 4CIPRO XR
06 9CIPROFLOXACIN EXTENDED RELEASE
07 65CIPROFLOXACIN HYDROCHLORIDE
08 1CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE
09 1OTOVEL
10 1PROQUIN XR
01 78No
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Dosage Strength : EQ 750MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 212.6MG;EQ 287.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 425.2MG;EQ 574.9MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : AB
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 : AB
