Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
01 4Taro Pharmaceutical Industries
02 2Bal Pharma
03 12care4 ApS
04 2ANI Pharmaceuticals Inc
05 3Accord healthcare
06 2Acme Lifetech
07 7Actavis Inc
08 3AiPing Pharmaceutical Inc
09 2Alcon Inc
10 1Altaire Pharmaceuticals
11 6Amneal Pharmaceuticals
12 1Amring Pharma
13 1Arya Pharma (Pty) Ltd
14 2Auro Pharma Inc
15 3Aurobindo Pharma Limited
16 1BIOMED 2002 INC
17 3Barr Laboratories
18 7Bayer AG
19 12Bio Labs
20 1Biodeal Pharmaceuticals
21 3Bluefish Pharmaceuticals AB
22 3Carlsbad Technology
23 3Chartwell Pharmaceuticals llc
24 1Cifarma
25 1DEPOMED INC
26 3Drug Medical Supplies Ltd.
27 2ENDO OPERATIONS
28 1Eloge
29 1Enlie Pharmaceutical Joint Stock Company
30 1FDC
31 4Focelite
32 1Fosun Pharmaceutical
33 2Halewood Laboratories Pvt. Ltd
34 2Hanlim Pharmaceuticals Inc
35 3Hexal AG
36 1Hi-Tech Pharma
37 3Hikma Pharmaceuticals
38 3IVAX Pharmaceuticals Inc
39 2JAMP PHARMA
40 3KRKA Sweden AB
41 1Key Therapeutics
42 1LABORATOIRE RIVA INC.
43 2Laboratorios Salvat
44 2MARCAN PHARMACEUTICALS INC
45 1MEDEXUS PHARMACEUTICALS INC.
46 1MINT PHARMACEUTICALS INC
47 1Medivision
48 3Natco Pharma
49 2Navamedic
50 2Neopharma
51 1Nora Pharma
52 2NoroBio Pharmaceutical
53 3Nostrum Laboratories
54 3Novartis Pharmaceuticals Corporation
55 3Novell Pharmaceutical Laboratories
56 1ORIFARM GROUP AS
57 1Opes Health Care
58 2PRO DOC LIMITEE
59 2PRO.MED.CS Praha
60 3Paranova Group AS
61 6Pharmascience Inc.
62 3Pliva Hrvatska
63 1RANBAXY LABORATORIES LIMITED
64 2Remedy Pharma
65 6Rising Pharmaceuticals Inc
66 1Rubicon Research
67 2SA Alcon Couvreur NV
68 1SANIS HEALTH INC
69 2SIVEM PHARMACEUTICALS ULC
70 8Sandoz B2B
71 1ScieGen Pharmaceuticals
72 6Sun Pharmaceutical Industries Limited
73 6Teva Pharmaceutical Industries
74 1The J. Molner Company
75 2Umedica Laboratories
76 3Unique Biotech Limited
77 4Viatris
78 1Virjo Healthcare
79 1World Medicine
80 5XYZ Pharma
81 1Yangtze River Pharmaceutical Group
82 2Yiling Pharmaceutical
83 3Zim Laboratories
01 2CAPSULE
02 1Capsule
03 3DC Granules and Tablets
04 2DRY POWDER SUSPENSION
05 1EAR DROPS
06 4EAR DROPS, SOLUTION
07 1EAR DROPS, SOLUTION IN SINGLE-DOSE CONTAINERS
08 1EYE DROP
09 1EYE DROPS
10 3EYE DROPS, SOLUTION
11 1EYE OINTMENT
12 1Eye Drops
13 4Eye Ointment
14 26FILM COATED PILL
15 3Film Coated Tablet
16 2Injection
17 1OINTMENT
18 1OINTMENT;OPHTHALMIC
19 1OPD
20 1Powder
21 3SOLUTION
22 9SOLUTION/DROPS;OPHTHALMIC
23 2SOLUTION/DROPS;OTIC
24 4SUSPENSION
25 1SUSPENSION/DROPS;OTIC
26 2Solution for infusion
27 1TAB
28 40TABLET
29 2TABLET, EXTENDED RELEASE; ORAL
30 12TABLET, EXTENDED RELEASE;ORAL
31 59TABLET;ORAL
32 14Tablet
33 1Tablet IP
34 1XR TABLET
35 1Blank
01 38DISCN
02 23Generic
03 37Prescription
04 46RX
05 68Blank
01 3ACT CIPROFLOXACIN
02 2AURO-CIPROFLOXACIN
03 1BIO-CIPROFLOXACIN
04 1Biofloxx 500
05 1C-Flox
06 1C-Oxacin
07 2C-Oxacin
08 1CETRAXAL
09 4CILOXAN
10 3CIPRO
11 1CIPRO HC
12 4CIPRO XR
13 1CIPROCIN HC
14 1CIPRODEX
15 3CIPROFLOXACIN
16 9CIPROFLOXACIN EXTENDED RELEASE
17 64CIPROFLOXACIN HYDROCHLORIDE
18 2CIPROXIN
19 1Ceprolen Eye Drop
20 1Cetraxal
21 2Cifloxinal
22 8Ciloxan
23 2Cipflox
24 3Ciprobio
25 4Ciprobio
26 1Ciprocin
27 3Ciprofloxacin Accord
28 3Ciprofloxacin Actavis
29 3Ciprofloxacin Amneal
30 3Ciprofloxacin Bluefish
31 3Ciprofloxacin Hexal
32 3Ciprofloxacin MDS
33 4Ciprofloxacin Mylan
34 2Ciprofloxacin Navamedic
35 1Ciprofloxacin Ranbaxy
36 3Civell
37 1Cypcino
38 1Eloge Cipro
39 2JAMP-CIPROFLOXACIN
40 2MAR-CIPROFLOXACIN
41 1MINT-CIPROFLOX
42 1Mediflox
43 1NRA-CIPROFLOXACIN
44 2Neocipro
45 1OTIXAL
46 1OTOVEL
47 6PMS-CIPROFLOXACIN
48 2PRO-CIPROFLOXACIN
49 1PROQUIN XR
50 1RIVA-CIPROFLOXACIN
51 4SANDOZ CIPROFLOXACIN
52 1SANDOZ CIPROFLOXACIN / DEXAMETHASONE
53 3TARO-CIPROFLOX
54 1TARO-CIPROFLOXACIN/DEXAMETHASONE
55 2Ultraflox
56 3ciprofloxacin Krka
57 21Blank
01 1Brazil
02 37Canada
03 3China
04 2Czech Republic
05 22India
06 3Indonesia
07 1Italy
08 2Norway
09 12Pakistan
10 2South Africa
11 2South Korea
12 35Sweden
13 1Turkey
14 2U.A.E
15 86USA
16 1Vietnam
Regulatory Info : Generic
Registration Country : India
Brand Name : Ultraflox
Dosage Form : Tablet
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2004-10-06
Application Number : 76912
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2004-10-06
Application Number : 76912
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 750MG BASE
Packaging :
Approval Date : 2004-10-06
Application Number : 76912
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE)
Brand Name : TARO-CIPROFLOXACIN/DEXAMETHASONE
Dosage Form : SUSPENSION
Dosage Strength : 0.3%/W/V
Packaging : 7.5ML
Approval Date :
Application Number : 2481901
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Generic
Registration Country : India
Brand Name : Ultraflox
Dosage Form : Tablet
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 74124
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 74124
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 750MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 74124
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CIPRO
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 1987-10-22
Application Number : 19537
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CIPRO
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1987-10-22
Application Number : 19537
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1987-10-22
Application Number : 19537
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 2002-12-13
Application Number : 21473
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 2003-08-28
Application Number : 21473
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : USA
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Brand Name : CIPRO XR
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Dosage Strength : 212.6MG; EQ 287.5MG BASE
Packaging :
Approval Date :
Application Number : 21554
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Brand Name : CIPRO XR
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Dosage Strength : 425.2MG; EQ 574.9MG BASE
Packaging :
Approval Date :
Application Number : 21554
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROQUIN XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2005-05-19
Application Number : 21744
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CETRAXAL
Dosage Form : SOLUTION/DROPS;OTIC
Dosage Strength : EQ 0.2% BASE
Packaging :
Approval Date : 2009-05-01
Application Number : 21918
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 750MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75685
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75685
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75685
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CILOXAN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.3% BASE
Packaging :
Approval Date : 1990-12-31
Application Number : 19992
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CILOXAN
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 0.3% BASE
Packaging :
Approval Date : 1998-03-30
Application Number : 20369
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE
Brand Name : CIPRO HC
Dosage Form : SUSPENSION/DROPS;OTIC
Dosage Strength : EQ 0.2% BASE;1%
Packaging :
Approval Date : 1998-02-10
Application Number : 20805
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75747
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75747
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 750MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75747
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 750MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75593
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75593
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CIPROFLOXACIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2004-06-09
Application Number : 75593
Regulatory Info : RX
Registration Country : USA
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