Fresenius Kabi USA Unclassified
FDA Approved Drugs
Fresenius Kabi USA Unclassified
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 18
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
Company Overview
Company
Fresenius Kabi USA Unclassified
Country
U.S.A
Website
Social Profiles
Company Snapshot
Fresenius Kabi USA Unclassified
Three Corporate DriveLake Zurich, Illinois 60047
U.S.A
www.fresenius-kabi.com/us/ contactus@fresenius-kabi.com View on MapFDA Approved Drug Records ( 18 records )
Drug Name
BENDAMUSTINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/4ML (25MG/ML)
Approval Date
-
Active Ingredient
BENDAMUSTINE HYDROCHLORIDE
Application Number
210410
Product Number
1
Dosage Form
-
Strength
100MG/4ML (25MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CABAZITAXEL
Product Number
1
Dosage Form
-
Strength
20MG/ML
Approval Date
-
Active Ingredient
CABAZITAXEL
Application Number
207937
Product Number
1
Dosage Form
-
Strength
20MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CHORIONIC GONADOTROPIN
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/VIAL
Approval Date
-
Active Ingredient
GONADOTROPIN, CHORIONIC
Application Number
17067
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CHORIONIC GONADOTROPIN
Product Number
2
Dosage Form
-
Strength
10,000 UNITS/VIAL
Approval Date
-
Active Ingredient
GONADOTROPIN, CHORIONIC
Application Number
17067
Product Number
2
Dosage Form
-
Strength
10,000 UNITS/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CHORIONIC GONADOTROPIN
Product Number
3
Dosage Form
-
Strength
20,000 UNITS/VIAL
Approval Date
-
Active Ingredient
GONADOTROPIN, CHORIONIC
Application Number
17067
Product Number
3
Dosage Form
-
Strength
20,000 UNITS/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CHORIONIC GONADOTROPIN
Product Number
4
Dosage Form
-
Strength
15,000 UNITS/VIAL
Approval Date
-
Active Ingredient
GONADOTROPIN, CHORIONIC
Application Number
17067
Product Number
4
Dosage Form
-
Strength
15,000 UNITS/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DEXMEDETOMIDINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)
Approval Date
-
Active Ingredient
DEXMEDETOMIDINE HYDROCHLORIDE
Application Number
208129
Product Number
4
Dosage Form
-
Strength
EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
GEMCITABINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 200MG BASE/VIAL
Approval Date
-
Active Ingredient
GEMCITABINE HYDROCHLORIDE
Application Number
90242
Product Number
1
Dosage Form
-
Strength
EQ 200MG BASE/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
GEMCITABINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
-
Active Ingredient
GEMCITABINE HYDROCHLORIDE
Application Number
90242
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IDACIO
Product Number
1
Dosage Form
-
Strength
40MG/0.8ML
Approval Date
-
Active Ingredient
ADALIMUMAB-AACF
Application Number
761255
Product Number
1
Dosage Form
-
Strength
40MG/0.8ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OTULFI
Product Number
1
Dosage Form
-
Strength
45MG/0.5ML
Approval Date
-
Active Ingredient
USTEKINUMAB-AAUZ
Application Number
761379
Product Number
1
Dosage Form
-
Strength
45MG/0.5ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OTULFI
Product Number
2
Dosage Form
-
Strength
90MG/1ML
Approval Date
-
Active Ingredient
USTEKINUMAB-AAUZ
Application Number
761379
Product Number
2
Dosage Form
-
Strength
90MG/1ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OTULFI
Product Number
3
Dosage Form
-
Strength
130MG/26ML
Approval Date
-
Active Ingredient
USTEKINUMAB-AAUZ
Application Number
761379
Product Number
3
Dosage Form
-
Strength
130MG/26ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
STIMUFEND
Product Number
1
Dosage Form
-
Strength
6MG/0.6ML
Approval Date
-
Active Ingredient
PEGFILGRASTIM-FPGK
Application Number
761173
Product Number
1
Dosage Form
-
Strength
6MG/0.6ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TYENNE
Product Number
2
Dosage Form
-
Strength
80MG/4ML
Approval Date
-
Active Ingredient
TOCILIZUMAB-AAZG
Application Number
761275
Product Number
2
Dosage Form
-
Strength
80MG/4ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TYENNE
Product Number
3
Dosage Form
-
Strength
200MG/10ML
Approval Date
-
Active Ingredient
TOCILIZUMAB-AAZG
Application Number
761275
Product Number
3
Dosage Form
-
Strength
200MG/10ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TYENNE
Product Number
4
Dosage Form
-
Strength
400MG/20ML
Approval Date
-
Active Ingredient
TOCILIZUMAB-AAZG
Application Number
761275
Product Number
4
Dosage Form
-
Strength
400MG/20ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TYENNE
Product Number
4
Dosage Form
-
Strength
162MG/0.9ML
Approval Date
-
Active Ingredient
TOCILIZUMAB-AAZG
Application Number
761449
Product Number
4
Dosage Form
-
Strength
162MG/0.9ML
Approval Date
-
Regulatory Status
Unclassified
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Drug Status Breakdown
18 total- Unclassified
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
Visit FDA Orange BookFDA Approved Drug Record Details Preview
Explore important FDA approved drug information available in the records above.
Drug Name
BENDAMUSTINE HYDROCHLORIDE
Application Number
210410
Product Number
1
Active Ingredient
BENDAMUSTINE HYDROCHLORIDE
Dosage Form
-
Strength
100MG/4ML (25MG/ML)
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