01 2AAIPharma Services Corp.
02 2ACME Laboratories
03 2ANI Pharmaceuticals Inc
04 2Actavis Inc
05 2Amneal Pharmaceuticals
06 1Bioindustria L.I.M. Spa
07 1CONTINENTAL PHARMA INC.
08 2Exela Pharma Sciences, LLC.
09 1Exelgyn, Paris
10 1Ferring Läkemedel AB
11 1Ferring Pharmaceuticals
12 2Genmed A Division Of Pfizer Canada Inc
13 1Infugen Pharma
14 1Linepharma
15 1MS Health
16 2Madras Pharmaceuticals
17 4Micro Labs Limited
18 2Novel Laboratories, Inc.
19 1Novell Pharmaceutical Laboratories
20 2Opes Health Care
21 23Pfizer Inc
22 4Pharmascience Inc.
23 2Sandoz B2B
24 2Yung Shin Pharmaceutical Industrial
25 2Zhejiang Xianju Pharmaceutical Co. Ltd
26 2Zydus Pharmaceuticals
01 1Antic-calc Tablet
02 6Bitabs
03 1KIT
04 1Misoprostol 200Mcg 50 Combined Oral Use
05 5TAB
06 6TABLET
07 6TABLET (DELAYED-RELEASE)
08 16TABLET, DELAYED RELEASE;ORAL
09 10TABLET;ORAL
10 2Tabl
11 9Tablet
12 1VAGINALINLÄGG
13 1Vaginal Posts
14 1tablet
15 2Blank
01 8DISCN
02 2Generic
03 3Originator
04 11Prescription
05 18RX
06 26Blank
01 2ARTHROTEC
02 1ARTHROTEC 50
03 1ARTHROTEC 75
04 5Arthrotec 50
05 4Arthrotec 75
06 1Artrotec
07 2CYTOTEC
08 6Cytotec
09 14DICLOFENAC SODIUM AND MISOPROSTOL
10 1GD-DICLOFENAC/MISOPROSTOL 50
11 1GD-DICLOFENAC/MISOPROSTOL 75
12 1MIFEGYMISO
13 10MISOPROSTOL
14 1MS-2 Step
15 2Misodel
16 1Misofenac
17 2Misoprostol Pfizer
18 1Noprostol
19 2PMS-DICLOFENAC-MISOPROSTOL
20 1PMS-MISOPROSTOL (0.1MG)
21 1PMS-MISOPROSTOL (0.2MG)
22 1Topogyne
23 7Blank
01 1Australia
02 11Canada
03 2China
04 5India
05 1Indonesia
06 3Italy
07 3Norway
08 5South Africa
09 3Sweden
10 8Switzerland
11 26USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2019-07-02
Application Number : 210201
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 2019-07-02
Application Number : 210201
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2012-07-09
Application Number : 201089
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2012-07-09
Application Number : 201089
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2016-11-25
Application Number : 203995
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2016-11-25
Application Number : 203995
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2002-07-10
Application Number : 76095
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 2002-07-10
Application Number : 76095
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2014-03-14
Application Number : 200540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2014-03-14
Application Number : 200540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2021-07-15
Application Number : 204355
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2021-07-15
Application Number : 204355
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2022-10-17
Application Number : 216872
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 2022-10-17
Application Number : 216872
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2012-07-25
Application Number : 91667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MISOPROSTOL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 2012-07-25
Application Number : 91667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CYTOTEC
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 1988-12-27
Application Number : 19268
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CYTOTEC
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 1990-09-21
Application Number : 19268
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : ARTHROTEC
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 1997-12-24
Application Number : 20607
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : ARTHROTEC
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 1997-12-24
Application Number : 20607
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Cytotec
Dosage Form : TABLET
Dosage Strength : 0.2 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MISOPROSTOL (0.1MG)
Dosage Form : TABLET
Dosage Strength : 0.1MG
Packaging : 100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2013-05-09
Application Number : 200158
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2013-05-09
Application Number : 200158
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2020-02-19
Application Number : 205143
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2020-02-19
Application Number : 205143
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 50MG;0.2MG
Packaging :
Approval Date : 2023-06-12
Application Number : 206771
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DICLOFENAC SODIUM; MISOPROSTOL
Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form : TABLET, DELAYED RELEASE;ORAL
Dosage Strength : 75MG;0.2MG
Packaging :
Approval Date : 2023-06-12
Application Number : 206771
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Misodel
Dosage Form : VAGINALINLÄGG
Dosage Strength : 200 MIKROGRAM
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Sweden
Brand Name : Topogyne
Dosage Form : TABLET
Dosage Strength : 400 MICROGRAM
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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