All the information on this site is from our Global Pharmaceutical Database.

other preparations, combinations

North America

Canada (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
HEMORRHOIDAL RELIEF OINTMENT 0.25% oint
OTC
topical
C05AX03
Perrigo
PREPARATION H-PE GEL (0.25%+50%) gel
OTC
rectal/topical
C05AX03
GlaxoSmithKline
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
HEMORRHOIDAL RELIEF OINTMENT 0.25% oint
02230466
Perrigo
PREPARATION H-PE GEL (0.25%+50%) gel
02209594
GlaxoSmithKline
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United States (0)
No result.

Europe

Austria (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
HäDENSA oint
OTC
-
C05AX03
Merz
HäDENSA ZäPFCHEN -
OTC
-
C05AX03
Merz
SPERTI PREPARATION H HäMORRHOIDALSALBE -
OTC
-
C05AX03
Pfizer
SPERTI PREPARATION H HäMORRHOIDALZäPFCHEN -
OTC
-
C05AX03
Pfizer
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
HäDENSA oint
2465
30-10-1972
Merz
HäDENSA ZäPFCHEN -
10746
10-09-1959
Merz
SPERTI PREPARATION H HäMORRHOIDALSALBE -
12944
12-03-1984
Pfizer
SPERTI PREPARATION H HäMORRHOIDALZäPFCHEN -
12945
12-03-1984
Pfizer
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Belgium (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLOPROCT CREME 0,1 % - 2 % rectal cream
10 g
15 g
30 g
Y
Y
Y


cut/rectal
C05AX03
Bayer
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLOPROCT CREME 0,1 % - 2 % rectal cream
10 g
15 g
30 g
BE270006
BE270006
BE270006
-
-
-
Bayer
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DOLOPROCT CREME 0,1 % - 2 % rectal cream
10 g
15 g
30 g
Bayer
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Croatia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
FAKTU 100 MG/2,5 MG I supp
10 suppa u stripu
Y
Rx
-
C05AX03
Takeda
FAKTU 50 MG/10 MG/G ZA REKTUM oint
1 tuba 20 g ointi i aplikator
Y
Rx
-
C05AX03
Takeda
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
FAKTU 100 MG/2,5 MG I supp
10 suppa u stripu
HR-H-179313303-01
30-06-2016
Takeda
FAKTU 50 MG/10 MG/G ZA REKTUM oint
1 tuba 20 g ointi i aplikator
HR-H-281798900-01
30-06-2016
Takeda
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Czechia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PREPARATION H 10MG/G+30MG/G rectal oint
10MG/G+30MG/G 25G
10MG/G+30MG/G 50G
Y
N
rectal
C05AX03
Pfizer
PREPARATION H 23MG/69MG supp
23MG/69MG 12
23MG/69MG 24
23MG/69MG 48
23MG/69MG 6
Y
N
N
N
rectal
C05AX03
Pfizer
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PREPARATION H 10MG/G+30MG/G rectal oint
10MG/G+30MG/G 25G
10MG/G+30MG/G 50G
23/ 215/90-C
23/ 215/90-C
NP
NP
Pfizer
PREPARATION H 23MG/69MG supp
23MG/69MG 12
23MG/69MG 24
23MG/69MG 48
23MG/69MG 6
23/ 216/90-C
23/ 216/90-C
23/ 216/90-C
23/ 216/90-C
NP
NP
NP
NP
Pfizer
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
PREPARATION H 10MG/G+30MG/G rectal oint
10MG/G+30MG/G 25G
10MG/G+30MG/G 50G
0
0
Pfizer
PREPARATION H 23MG/69MG supp
23MG/69MG 12
23MG/69MG 24
23MG/69MG 48
23MG/69MG 6
0
0
0
0
Pfizer
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Denmark (0)
No result.
Hungary (4)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
REPARON rectal oint
1x25g al tube
1x30g al tube
1x40g al tube
Y
Y
N
OTC
OTC
OTC
-
C05AX03
Egis
REPARON supp
10x foil
12x foil
Y
Y
OTC
OTC
rectal
C05AX03
Egis
SPERTI PREPARATION H rectal oint
1x25g al tube
Y
OTC
rectal
C05AX03
Pfizer
SPERTI PREPARATION H supp
12x szalagcsomagolásban
Y
OTC
rectal
C05AX03
Pfizer
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
REPARON rectal oint
1x25g al tube
1x30g al tube
1x40g al tube
OGYI-T-09005/01
OGYI-T-09005/04
OGYI-T-09005/05
12-08-2003
12-08-2003
12-08-2003
Egis
REPARON supp
10x foil
12x foil
OGYI-T-09005/02
OGYI-T-09005/03
12-08-2003
12-08-2003
Egis
SPERTI PREPARATION H rectal oint
1x25g al tube
OGYI-T-21820/02
25-08-2011
Pfizer
SPERTI PREPARATION H supp
12x szalagcsomagolásban
OGYI-T-21820/01
25-08-2011
Pfizer
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
REPARON rectal oint
1x25g al tube
1x30g al tube
1x40g al tube
0
0
0
0
0
0
0
0
0
0
0
0
Egis
REPARON supp
10x foil
12x foil
0
0
0
0
0
0
0
0
Egis
SPERTI PREPARATION H rectal oint
1x25g al tube
0
0
0
0
Pfizer
SPERTI PREPARATION H supp
12x szalagcsomagolásban
0
0
0
0
Pfizer
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Iceland (0)
No result.
Ireland (0)
No result.
Lithuania (0)
No result.
Malta (10)
X
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ANACAL rectal oint
MA085/00301
11-08-2006
Genus Pharmaceuticals
ANACAL SUPPOSITORIES supp
MA085/00302
11-08-2006
Genus Pharmaceuticals
ANODESYN oint
AA055/01002
05-02-2009
Thornton & Ross
ANODESYN SUPPOSITORIES supp
AA055/01001
05-02-2009
Thornton & Ross
ANTROLIN 0.3% + 1.5% rectal cream
AA943/00102
23-02-2016
New.Fa.Dem.
DOLOPROCT 0.1% + 2% rectal cream
MA1013/00102
28-09-2005
Jenapharm
DOLOPROCT 1MG + 40MG SUPPOSITORIES supp
MA1013/00101
28-09-2005
Jenapharm
PROCTO-GLYVENOL 5%W/W, 2%W/W rectal cream
MA1177/01101
23-07-2008
GlaxoSmithKline
PROCTOSEDYL oint
MA082/02201
28-09-2005
Sanofi
PROCTOSEDYL supp
MA082/02202
28-09-2005
Sanofi
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Poland (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PROCTO-HEMOLAN (50 MG + 20 MG)/G rectal cream
1 tube 20 g
1 tube 30 g
OTC
OTC
-
C05AX03
Aflofarm Farmacja
PROCTO-HEMOLAN 400 MG + 40 MG supp
10 sachet
OTC
-
C05AX03
Aflofarm Farmacja
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PROCTO-HEMOLAN (50 MG + 20 MG)/G rectal cream
1 tube 20 g
1 tube 30 g
11671
11671
NP
NP
Aflofarm Farmacja
PROCTO-HEMOLAN 400 MG + 40 MG supp
10 sachet
22098
NP
Aflofarm Farmacja
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Romania (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
PROCTOLIZIN 10 MG/20 MG/50 MG PE GRAM cream
1 tubee Al x 25 g cream
-
P-RF
-
C05AX03
Fiterman Pharma
PROCTOLOG 120MG/10MG SUPOZ.
2 folii din PVC/PE x 5 supoz.
-
OTC
-
C05AX03
Pfizer
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
PROCTOLIZIN 10 MG/20 MG/50 MG PE GRAM cream
1 tubee Al x 25 g cream
-
Fiterman Pharma
PROCTOLOG 120MG/10MG SUPOZ.
2 folii din PVC/PE x 5 supoz.
-
Pfizer
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Slovenia (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
DOLOPROCT 1 MG/20 MG V 1 G rectal cream
tubo 10 g kreme
tubo 15 g kreme
tubo 30 g kreme
-
N
-
Rx
Rx
Rx
rectal
C05AX03
Leo
DOLOPROCT 1 MG/40 MG supp
10 suppmi (2 x 5 svečk dvojnem traku)
120 suppmi (24 x 5 svečk dvojnem traku)
N
-
Rx
Rx
rectal
C05AX03
Leo
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
DOLOPROCT 1 MG/20 MG V 1 G rectal cream
tubo 10 g kreme
tubo 15 g kreme
tubo 30 g kreme
103-84/2019-4
103-84/2019-4
103-84/2019-4
MRP
MRP
MRP
17-01-2020
17-01-2020
17-01-2020
Leo
DOLOPROCT 1 MG/40 MG supp
10 suppmi (2 x 5 svečk dvojnem traku)
120 suppmi (24 x 5 svečk dvojnem traku)
103-84/2019-4
103-84/2019-4
MRP
MRP
17-01-2020
17-01-2020
Leo
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
DOLOPROCT 1 MG/20 MG V 1 G rectal cream
tubo 10 g kreme
tubo 15 g kreme
tubo 30 g kreme
Leo
DOLOPROCT 1 MG/40 MG supp
10 suppmi (2 x 5 svečk dvojnem traku)
120 suppmi (24 x 5 svečk dvojnem traku)
Leo
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Spain (7)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
ANSO rectal oint
1 tube of 50 g
Y
OTC
rectal
C05AX03
Lacer
DOLOPROCT 1 MG/40 MG S supp
10 supp
-
OTC
rectal
C05AX03
Bayer
DOLOPROCT 1 MG/G + 20 MG/G rectal cream
1 tube of 30 g
-
OTC
rectal
C05AX03
Bayer
HADENSA rectal oint
1 tube of 42 g
-
OTC
rectal
C05AX03
Ferrer
HADENSA S supp
10 supp
-
OTC
rectal
C05AX03
Ferrer
PROCTOLOG rectal oint
1 tube of 15 g
1 tube of 30 g
Y
Y
OTC
OTC
rectal
C05AX03
Desma
PROCTOLOG S supp
10 supp
Y
Rx
rectal
C05AX03
Desma
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ANSO rectal oint
1 tube of 50 g
51967
01-01-1974
Lacer
DOLOPROCT 1 MG/40 MG S supp
10 supp
65986
25-03-2004
Bayer
DOLOPROCT 1 MG/G + 20 MG/G rectal cream
1 tube of 30 g
65985
31-03-2004
Bayer
HADENSA rectal oint
1 tube of 42 g
21899
01-10-1954
Ferrer
HADENSA S supp
10 supp
29087
01-04-1958
Ferrer
PROCTOLOG rectal oint
1 tube of 15 g
1 tube of 30 g
54647
54647
01-11-1979
01-11-1979
Desma
PROCTOLOG S supp
10 supp
54648
01-12-1979
Desma
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Sweden (2)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
ALCOSANAL 110 MG/G rectal oint
OTC
-
C05AX03
Meda
ALCOSANAL 200 MG supp
OTC
-
C05AX03
Meda
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
ALCOSANAL 110 MG/G rectal oint
Nationell decentral eller ömsesidig
19-12-1957
Meda
ALCOSANAL 200 MG supp
Nationell decentral eller ömsesidig
19-12-1957
31-01-2018
Meda
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Switzerland (1)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
HAMETUM-HAEMO supp
-
D
-
C05AX03
Schwabe
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
HAMETUM-HAEMO supp
65855 1
Hauptzulassung
20-08-2015
Schwabe
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Data source