ACS DOBFAR SPA RX
FDA Approved Drugs
ACS DOBFAR SPA RX
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 31
- Latest Approval Date Oct 26, 2018
- Data Source FDA
- First Approval Date Nov 20, 1985
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ACS DOBFAR SPA RX
Viale Addetta 4/12 20067 Tribiano (Milan)
Italy
www.acsdobfar.it/ info@acsdobfar.it View on MapFDA Approved Drug Records ( 31 records )
Drug Name
AMPICILLIN AND SULBACTAM
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Approval Date
2009-12-23
Active Ingredient
AMPICILLIN SODIUM; SULBACTAM SODIUM
Application Number
65403
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Approval Date
2009-12-23
Regulatory Status
RX
Drug Name
AMPICILLIN AND SULBACTAM
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Approval Date
2009-12-22
Active Ingredient
AMPICILLIN SODIUM; SULBACTAM SODIUM
Application Number
65406
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Approval Date
2009-12-22
Regulatory Status
RX
Drug Name
AMPICILLIN AND SULBACTAM
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Approval Date
2009-12-22
Active Ingredient
AMPICILLIN SODIUM; SULBACTAM SODIUM
Application Number
65406
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Approval Date
2009-12-22
Regulatory Status
RX
Drug Name
AMPICILLIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2013-04-03
Active Ingredient
AMPICILLIN SODIUM
Application Number
90889
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2013-04-03
Regulatory Status
RX
Drug Name
CEFAZOLIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2008-10-22
Active Ingredient
CEFAZOLIN SODIUM
Application Number
65303
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2008-10-22
Regulatory Status
RX
Drug Name
CEFAZOLIN SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-10-22
Active Ingredient
CEFAZOLIN SODIUM
Application Number
65303
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-10-22
Regulatory Status
RX
Drug Name
CEFAZOLIN SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2008-10-22
Active Ingredient
CEFAZOLIN SODIUM
Application Number
65306
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2008-10-22
Regulatory Status
RX
Drug Name
CEFAZOLIN SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 20GM BASE/VIAL
Approval Date
2014-08-18
Active Ingredient
CEFAZOLIN SODIUM
Application Number
65306
Product Number
2
Dosage Form
-
Strength
EQ 20GM BASE/VIAL
Approval Date
2014-08-18
Regulatory Status
RX
Drug Name
CEFEPIME HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-03-20
Active Ingredient
CEFEPIME HYDROCHLORIDE
Application Number
65441
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-03-20
Regulatory Status
RX
Drug Name
CEFEPIME HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2008-03-20
Active Ingredient
CEFEPIME HYDROCHLORIDE
Application Number
65441
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2008-03-20
Regulatory Status
RX
Drug Name
CEFOXITIN
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2009-06-12
Active Ingredient
CEFOXITIN SODIUM
Application Number
65414
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2009-06-12
Regulatory Status
RX
Drug Name
CEFOXITIN
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2009-06-12
Active Ingredient
CEFOXITIN SODIUM
Application Number
65414
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2009-06-12
Regulatory Status
RX
Drug Name
CEFOXITIN
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2010-05-19
Active Ingredient
CEFOXITIN SODIUM
Application Number
65415
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2010-05-19
Regulatory Status
RX
Drug Name
CEFTAZIDIME
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1985-11-20
Active Ingredient
CEFTAZIDIME
Application Number
62640
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1985-11-20
Regulatory Status
RX
Drug Name
CEFTAZIDIME
Product Number
3
Dosage Form
-
Strength
2GM/VIAL
Approval Date
1985-11-20
Active Ingredient
CEFTAZIDIME
Application Number
62640
Product Number
3
Dosage Form
-
Strength
2GM/VIAL
Approval Date
1985-11-20
Regulatory Status
RX
Drug Name
CEFTAZIDIME
Product Number
4
Dosage Form
-
Strength
6GM/VIAL
Approval Date
1992-02-03
Active Ingredient
CEFTAZIDIME
Application Number
62640
Product Number
4
Dosage Form
-
Strength
6GM/VIAL
Approval Date
1992-02-03
Regulatory Status
RX
Drug Name
CEFTRIAXONE
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2008-07-24
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65328
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2008-07-24
Regulatory Status
RX
Drug Name
CEFTRIAXONE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2008-07-24
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65329
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2008-07-24
Regulatory Status
RX
Drug Name
CEFTRIAXONE
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-07-24
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65329
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2008-07-24
Regulatory Status
RX
Drug Name
CEFTRIAXONE
Product Number
3
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2008-07-24
Active Ingredient
CEFTRIAXONE SODIUM
Application Number
65329
Product Number
3
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2008-07-24
Regulatory Status
RX
Drug Name
CEFUROXIME SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 750MG BASE/VIAL
Approval Date
1997-05-30
Active Ingredient
CEFUROXIME SODIUM
Application Number
64125
Product Number
1
Dosage Form
-
Strength
EQ 750MG BASE/VIAL
Approval Date
1997-05-30
Regulatory Status
RX
Drug Name
CEFUROXIME SODIUM
Product Number
2
Dosage Form
-
Strength
EQ 1.5GM BASE/VIAL
Approval Date
1997-05-30
Active Ingredient
CEFUROXIME SODIUM
Application Number
64125
Product Number
2
Dosage Form
-
Strength
EQ 1.5GM BASE/VIAL
Approval Date
1997-05-30
Regulatory Status
RX
Drug Name
ERTAPENEM SODIUM
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2018-04-16
Active Ingredient
ERTAPENEM SODIUM
Application Number
208790
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2018-04-16
Regulatory Status
RX
Drug Name
IMIPENEM AND CILASTATIN
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL;250MG/VIAL
Approval Date
2011-12-21
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
90577
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL;250MG/VIAL
Approval Date
2011-12-21
Regulatory Status
RX
Drug Name
IMIPENEM AND CILASTATIN
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL;500MG/VIAL
Approval Date
2011-12-21
Active Ingredient
CILASTATIN SODIUM; IMIPENEM
Application Number
90577
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL;500MG/VIAL
Approval Date
2011-12-21
Regulatory Status
RX
Drug Name
MEROPENEM
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
2011-10-26
Active Ingredient
MEROPENEM
Application Number
91404
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
2011-10-26
Regulatory Status
RX
Drug Name
MEROPENEM
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
2011-10-26
Active Ingredient
MEROPENEM
Application Number
91404
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
2011-10-26
Regulatory Status
RX
Drug Name
MEROPENEM
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
2016-06-09
Active Ingredient
MEROPENEM
Application Number
204139
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
2016-06-09
Regulatory Status
RX
Drug Name
MEROPENEM
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
2016-06-09
Active Ingredient
MEROPENEM
Application Number
204139
Product Number
2
Dosage Form
-
Strength
1GM/VIAL
Approval Date
2016-06-09
Regulatory Status
RX
Drug Name
PENICILLIN G POTASSIUM
Product Number
1
Dosage Form
-
Strength
5,000,000 UNITS/VIAL
Approval Date
2018-10-26
Active Ingredient
PENICILLIN G POTASSIUM
Application Number
205043
Product Number
1
Dosage Form
-
Strength
5,000,000 UNITS/VIAL
Approval Date
2018-10-26
Regulatory Status
RX
Drug Name
PENICILLIN G POTASSIUM
Product Number
2
Dosage Form
-
Strength
20,000,000 UNITS/VIAL
Approval Date
2018-10-26
Active Ingredient
PENICILLIN G POTASSIUM
Application Number
205043
Product Number
2
Dosage Form
-
Strength
20,000,000 UNITS/VIAL
Approval Date
2018-10-26
Regulatory Status
RX
Drug Status Breakdown
31 total- RX
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Drug Name
AMPICILLIN AND SULBACTAM
Application Number
65403
Product Number
1
Active Ingredient
AMPICILLIN SODIUM; SULBACTAM SODIUM
Dosage Form
-
Strength
EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
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