Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
01 1Taro Pharmaceutical Industries
02 2Strides Pharma Science
03 1ANGITA PHARMA INC.
04 1Alcon Inc
05 1Aralez Pharmaceuticals
06 1Aurobindo Pharma Limited
07 7BRAINTREE LABS
08 1Bayer AG
09 1CellChem Pharmaceuticals
10 1Dynapharm
11 1E-Z-EM Canada Inc, dba Therapex
12 1Hanlim Pharmaceuticals Inc
13 1Hospira, Inc.
14 1JAMP PHARMA
15 2Johnson & Johnson
16 1Juno Pharmaceuticals Pty Ltd
17 1MANTRA PHARMA INC
18 1MEDEXUS PHARMACEUTICALS INC.
19 1Medisca
20 8NORVIUM BIOSCIENCE
21 1Norgine
22 1Nostrum Laboratories
23 6Novel Laboratories, Inc.
24 3PENDOPHARM DIVISION OF DE PHARMASCIENCE INC
25 4Perrigo Company plc
26 1Pharmascience Inc.
27 2Rising Pharmaceuticals Inc
28 2Salix Pharmaceuticals
29 1Sandoz B2B
30 1Teva API
31 1Teva Pharmaceutical Industries
32 2Vintage Pharmaceuticals-Charlotte
01 2DROPS
02 1EYE DROP
03 3FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL
04 28FOR SOLUTION;ORAL
05 6FOR SUSPENSION;ORAL
06 13POWDER FOR SOLUTION
07 2SOLUTION
08 1SOLUTION; ORAL AND TABLET; DELAYED RELEASE
09 2SOLUTION;ORAL
10 1TABLET (DELAYED-RELEASE)
11 1Blank
01 26DISCN
02 3Ethical
03 1Generic
04 15OTC
05 12RX
06 3Blank
01 1ADVANCED RELIEF EYE DROPS
02 1BI-PEGLYTE
03 1CLEARLAX
04 1CLENZ-LYTE
05 1CO-LAV
06 1COLOVAGE
07 6COLYTE
08 1COLYTE WITH FLAVOR PACKS
09 2COLYTE-FLAVORED
10 1COMFILAX
11 1CVS LUBRICANT
12 1E-Z-EM PREP LYTE
13 1EMOLAX
14 1GLYCOPREP
15 1GO-EVAC
16 2GOLYTELY
17 2HALFLYTELY
18 1HYDRALAX
19 1Kleanprep
20 1LAX-A-DAY
21 1LAX-A-DAY PHARMA
22 1LAX-LYTE WITH FLAVOR PACKS
23 1M-PEG 3350
24 2MOVIPREP
25 1NULYTELY
26 1NULYTELY-FLAVORED
27 1OCL
28 2PEG 3350
29 3PEG 3350 AND ELECTROLYTES
30 4PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE
31 1PEG-3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE AND BISACODYL
32 2PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID
33 1PEG-LYTE
34 1PLENVU
35 2POLYETHYLENE GLYCOL 3350 AND ELECTROLYTES
36 1POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL
37 1RED EYE TRIPLE ACTION
38 1RED EYE WORKPLACE
39 1RELAXA
40 1RESTORALAX
41 1SUCLEAR
42 1SYSTANE LUBRICANT EYE DROPS
43 1TRILYTE
01 18Canada
02 1Italy
03 1South Korea
04 40USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : RX
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : POLYETHYLENE GLYCOL 3350 AND ELECTROLYTES
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
Packaging :
Approval Date : 2018-12-21
Application Number : 204558
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
Brand Name : PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM
Packaging :
Approval Date : 2024-06-28
Application Number : 207498
Regulatory Info : RX
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : RX
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Brand Name : PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
Packaging :
Approval Date : 2015-04-13
Application Number : 204559
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : GOLYTELY
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
Packaging :
Approval Date : 1984-07-13
Application Number : 19011
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : GOLYTELY
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET
Packaging :
Approval Date : 1992-06-02
Application Number : 19011
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Brand Name : NULYTELY
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
Packaging :
Approval Date : 1991-04-22
Application Number : 19797
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Brand Name : NULYTELY-FLAVORED
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
Packaging :
Approval Date : 1994-11-18
Application Number : 19797
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : USA
BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Brand Name : HALFLYTELY
Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM
Packaging :
Approval Date :
Application Number : 21551
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Brand Name : HALFLYTELY
Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2010-07-16
Application Number : 21551
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : E-Z-EM PREP LYTE
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
Packaging :
Approval Date : 1988-11-21
Application Number : 71278
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE
Brand Name : OCL
Dosage Form : SOLUTION;ORAL
Dosage Strength : 6GM/100ML;75MG/100ML;168MG/100ML;146MG/100ML;1.29GM/100ML
Packaging :
Approval Date : 1986-04-30
Application Number : 19284
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE
Brand Name : MOVIPREP
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM
Packaging :
Approval Date : 2006-08-02
Application Number : 21881
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-10-26
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 120GM/PACKET;1.49GM/PACKET;3.36GM/PACKET;2.92GM/PACKET;11.36GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-10-26
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 360GM/PACKET;4.47GM/PACKET;10.08GM/PACKET;8.76GM/PACKET;34.08GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-10-26
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1987-06-12
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE-FLAVORED
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1991-11-14
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE-FLAVORED
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1991-11-14
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1989-01-31
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Brand Name : COLYTE WITH FLAVOR PACKS
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT
Packaging :
Approval Date : 1998-10-08
Application Number : 18983
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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