EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 9Sanofi
03 3Orion Corporation
04 1Ethypharm
05 3AFT Pharmaceuticals
06 1AMBICARE PHARMACEUTICALS INC.
07 1ANGITA PHARMA INC.
08 1Acme Lifetech
09 1Amavita Health Care Ag
10 2BRAINTREE LABS
11 1Celogen Pharma Pvt. Ltd
12 1Church & Dwight Co
13 1Coop Vitality Health Care Gmbh
14 1D & C MOBILITY SOLUTIONS INC.
15 1Emil Pharmaceutical
16 1G-Pharma Ag
17 1Glumex Pharmaceuticals Mfg. Pvt. Ltd
18 1Gracious Pharmaceutical
19 2Grindeks AS
20 1Halewood Laboratories Pvt. Ltd
21 1Holden Medical Laboratories Pvt. Ltd
22 1Indoco Remedies Limited
23 2Infugen Pharma
24 3JAMP PHARMA
25 1Juno Pharmaceuticals Pty Ltd
26 1Laboratorio Eczane Pharma
27 1Maxheal Pharmaceuticals (India) Ltd
28 1Medreich
29 2Meridian Enterprises Pvt. Ltd
30 1Mint Health Ltd
31 1National Pharma
32 2Novel Laboratories, Inc.
33 1ODAN LABORATORIES LTD
34 2Opel Healthcare Switzerland Ag
35 12Opella Healthcare Group
36 1Opes Health Care
37 2Paranova Pharmaceuticals Ab
38 1Pendopharm
39 10Petrus Pharmaceuticals
40 4Pharmascience Inc.
41 1Poddar Pharmaceuticals
42 1RELIANCE FORMULATION PVT. LTD
43 1Ravenbhel Pharma
44 1Remedica Limited
45 1Remedy Pharma
46 1Roha Arzneimittel Gmbh
47 1SCI SUPPLY INC.
48 3SIGMA LIFE SCIENCES INC.
49 1Sapps Pharmaceuticals
50 1Smith & Kenner Pharmaceuticals
51 2Streuli Pharma
52 1Sun Store Health Care Ag
53 1TIME-CAP LABORATORIES, INC
54 2Tentan Ag
55 1Trends Pharma
56 1VITA HEALTH PRODUCTS INC
57 2Vaishali Pharma Ltd
58 2Verfora
59 1XL Laboratories Private Limited
01 1Coated Tablet
02 1DR Tablet
03 2Enteric Coated Tablet
04 3FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL
05 1Film Coated Tablet
06 1Gastro Resistant Tablets
07 11Gastro-Resistant Tablet
08 2KIT
09 2Rectal Suspension
10 1SOLUTION; ORAL AND TABLET; DELAYED RELEASE
11 10SUPPOSITORY
12 1Suppositories
13 9Suppository
14 13TABLET
15 1TABLET (DELAYED-RELEASE)
16 1TABLET (ENTERIC-COATED)
17 31Tablet
18 18Blank
01 12Allowed
02 5Approved
03 3Authorised
04 7Authorized
05 1Cancelled
06 2DISCN
07 2Deregistered
08 2Ethical
09 6Generic
10 1Invalid
11 3Marketed
12 17NON-PRESCRIPTION DRUGS
13 4OTC
14 1Withdrawn
15 43Blank
01 1AMB-BISACODYL
02 1Amavita Bisacodyl-N
03 1BI-PEGLYTE
04 1BISACODYL
05 1BISACODYL LAXATIVE
06 2BISACODYL SUPPOSITORY
07 1BISACODYL TABLETS
08 1BISACODYL TABLETS 5MG
09 1BISACODYL TABLETS, 5 MG
10 1BISACODYL-ODAN
11 1BISACODYL-XL
12 1Bekunis
13 1Bekunis Drag?es Bisacodyl
14 1Bisacodyl
15 1Bisacodyl Grindeks
16 1Bisacodyl-Grindeks
17 1Bisacofelan
18 2Bisupp
19 1CARTER'S LITTLE PILLS
20 1CODULAX TABLETS
21 1Coop Vitality Bisacodyl-N
22 2DULCOLAX
23 1DULCOLAX FOR WOMEN
24 13Dulcolax
25 4Dulcolax Bisacodil
26 2Dulcolax Bisacodyl
27 1Dulcolax Twelve Plus
28 3Dulcolaxo Bisacodyl
29 2HALFLYTELY
30 1JAMP-BISACODYL
31 1JAMPLYTE + BISACODYL
32 1LAXATIVE FOR WOMEN
33 4Lax-Tab
34 1Medibudget Abf?hrdrag?es Bisacodyl
35 1Muxol N
36 1PEG-3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE AND BISACODYL
37 2PMS-BISACODYL
38 1POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL
39 10Petrus Bisacodyl Suppositories
40 2Prontolax
41 1SILVER BULLET SUPPOSITORY
42 1SOFLAX EX 10
43 1SOFLAX EX 5
44 1SUN STORE Bisacodyl
45 1Sapplax
46 1THE MAGIC BULLET
47 1Tavolax
48 4Toilax
49 1Ultralax
50 21Blank
01 1Argentina
02 18Australia
03 23Canada
04 25India
05 1Latvia
06 5Malta
07 1Moldova
08 3Norway
09 8Spain
10 7Sweden
11 12Switzerland
12 4USA
13 1Zimbabwe
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Dulcolaxo Bisacodyl
Dosage Form : Gastro-Resistant Tablet
Dosage Strength : 5MG
Packaging :
Approval Date : 2018-08-08
Application Number : PL04425-0718
Regulatory Info : Cancelled
Registration Country : Spain
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Dulcolaxo Bisacodyl
Dosage Form : Gastro-Resistant Tablet
Dosage Strength : 5MG
Packaging :
Approval Date : 2021-01-05
Application Number : 36881-28-7-2008
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Toilax
Dosage Form : Rectal Suspension
Dosage Strength : 10mg/5ml
Packaging :
Approval Date : 06/03/1970
Application Number : 19700306000015
Regulatory Info : Approved
Registration Country : Sweden
Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Bisacodyl
Dosage Form : Suppository
Dosage Strength : 10MG
Packaging :
Approval Date : 2007-10-01
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Brand Name : DULCOLAX
Dosage Form : TABLET (ENTERIC-COATED)
Dosage Strength : 5MG
Packaging : 10/30/60/100
Approval Date :
Application Number : 254142
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Brand Name : DULCOLAX
Dosage Form : SUPPOSITORY
Dosage Strength : 10MG
Packaging : 3/6/100
Approval Date :
Application Number : 3875
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Brand Name : DULCOLAX FOR WOMEN
Dosage Form : TABLET
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 2397854
Regulatory Info : NON-PRESCRIPTION DRUGS
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Australia
Brand Name : Dulcolax
Dosage Form :
Dosage Strength : 10 mg
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Australia
Brand Name : Dulcolax
Dosage Form :
Dosage Strength : 10 mg
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Australia
Brand Name : Dulcolax
Dosage Form :
Dosage Strength : 10 mg
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Australia
Brand Name : Dulcolax
Dosage Form :
Dosage Strength : 10 mg
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Australia
Brand Name : Dulcolax
Dosage Form :
Dosage Strength : 10 mg
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Toilax
Dosage Form : Tablet
Dosage Strength : 5mg
Packaging :
Approval Date : 28/03/1969
Application Number : 19690328000042
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Toilax
Dosage Form : Tablet
Dosage Strength : 5mg;10mg;5ml
Packaging :
Approval Date : 06/03/1970
Application Number : 19700306000022
Regulatory Info : Approved
Registration Country : Sweden
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 : Generic
Registration Country : India
Brand Name : Bisupp
Dosage Form : SUPPOSITORY
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : India
Brand Name : Bisupp
Dosage Form : SUPPOSITORY
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info :
Registration Country : USA
POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL
Brand Name : POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL
Dosage Form : SOLUTION; ORAL AND TABLET; DELAYED RELEASE
Dosage Strength : 2MG; 5MG
Packaging :
Approval Date :
Application Number : 90197
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Brand Name : PEG-3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE AND BISACODYL
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 : 2014-08-20
Application Number : 202217
Regulatory Info : DISCN
Registration Country : USA
