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Sultamicillin is a form of the antibiotic combination (codrug or mutual prodrug) ampicillin/sulbactam. Ampicillin belongs to a group of medicines called 'penicillins' and sulbactam belongs to a group of medicines called 'beta-lactam inhibitors'. Ampicillin / Sulbactam is indicated in the treatment of the following:
- community acquired pneumonia
- upper urinary tract infection
- intra-abdominal infections
- gynaecological infections
- skin and soft tissues infections
- Prophylaxis against infections associated with abdominal surgery
sultamicillin
For informational purposes only, X-Pharma does not provide medical advice.
SPC/PIL of the products can differ from this general indication.
J01CR04SPC/PIL of the products can differ from this general indication.
Sultamicillin is a form of the antibiotic combination (codrug or mutual prodrug) ampicillin/sulbactam. Ampicillin belongs to a group of medicines called 'penicillins' and sulbactam belongs to a group of medicines called 'beta-lactam inhibitors'. Ampicillin / Sulbactam is indicated in the treatment of the following:
- community acquired pneumonia
- upper urinary tract infection
- intra-abdominal infections
- gynaecological infections
- skin and soft tissues infections
- Prophylaxis against infections associated with abdominal surgery
North America
Canada (0)
No result.
United States (37)
X
Product
Pack
Market
Pres.
Dosage
ATC
Company
Y
Rx
INJECTION
J01CR04
Y
Rx
INJECTION
J01CR04
Y
Y
Y
Rx
Rx
Rx
INJECTION
J01CR04
N
INJECTION
J01CR04
Y
Rx
INJECTION
J01CR04
N
INJECTION
J01CR04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
90578/1
ANDA
11-01-2016
201406/1
ANDA
07-12-2015
90579/1
ANDA
08-01-2016
90349/1
90340/1
90340/1
ANDA
ANDA
ANDA
20-09-2010
20-09-2010
20-09-2010
90375/1
90653/1
90653/1
ANDA
ANDA
ANDA
21-12-2011
21-12-2011
21-12-2011
65316/1
ANDA
29-06-2007
65241/1
65310/1
65310/1
ANDA
ANDA
ANDA
25-07-2006
25-07-2006
25-07-2006
90579/2
ANDA
08-01-2016
90349/2
90340/2
90340/2
ANDA
ANDA
ANDA
20-09-2010
20-09-2010
20-09-2010
90375/2
90653/2
90653/2
ANDA
ANDA
ANDA
21-12-2011
21-12-2011
21-12-2011
65316/2
ANDA
29-06-2007
65241/2
65310/2
65310/2
ANDA
ANDA
ANDA
25-07-2006
25-07-2006
25-07-2006
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Europe
Austria (1)
X
Belgium (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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No result.
Croatia (0)
No result.
Czechia (1)
X
Denmark (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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No result.
Hungary (2)
X
Iceland (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
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No result.
Ireland (0)
No result.
Lithuania (3)
X
Malta (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
30 ml ir matavimo šaukštas, N1 bottle
60 ml ir matavimo šaukštas, N1 bottle
60 ml ir matavimo šaukštas, N1 bottle
Rx
Rx
Rx
oral
J01CR04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
30 ml ir matavimo šaukštas, N1 bottle
60 ml ir matavimo šaukštas, N1 bottle
60 ml ir matavimo šaukštas, N1 bottle
LT/1/96/1634/002
LT/1/96/1634/003
LT/1/96/1634/003
NP
NP
NP
17-05-1996
17-05-1996
17-05-1996
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No result.
Poland (1)
X
Romania (2)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Slovenia (2)Product
Pack
Market
Pres.
Dosage
ATC
Company
1 flac. din PEID cu pulbere pt. 60 ml su
-
PRF
-
J01CR04
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
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X
Spain (0)Product
Pack
Market
Pres.
Dosage
ATC
Company
Product
Pack
Reg. Nr.
Reg. Type
Reg. Date
Reg. Valid
Revocation
Company
Product
Pack
Ex-fact
Wholesale
Net retail
Gr. retail
Company
steklenička powd za pripravo 60 ml susp
10 tablet 375 mg
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No result.
Sweden (0)
No result.
Switzerland (0)
No result.
