Sandoz B2B Unclassified
FDA Approved Drugs
Sandoz B2B 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 50
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
Company Overview
Company
Sandoz B2B Unclassified
Country
Switzerland
Website
Social Profiles
Company Snapshot
Sandoz B2B Unclassified
Forum 1, Novartis Campus, CH-4056 Basel
Switzerland
www.sandoz.com/ sandoz.b2b@sandoz.com View on MapFDA Approved Drug Records ( 50 records )
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
-
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
85970
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
BIMATOPROST
Product Number
1
Dosage Form
-
Strength
0.03
Approval Date
-
Active Ingredient
BIMATOPROST
Application Number
200487
Product Number
1
Dosage Form
-
Strength
0.03
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CABAZITAXEL
Product Number
1
Dosage Form
-
Strength
45MG/4.5ML (10MG/ML)
Approval Date
-
Active Ingredient
CABAZITAXEL
Application Number
208715
Product Number
1
Dosage Form
-
Strength
45MG/4.5ML (10MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CABAZITAXEL
Product Number
2
Dosage Form
-
Strength
60MG/6ML (10MG/ML)
Approval Date
-
Active Ingredient
CABAZITAXEL
Application Number
208715
Product Number
2
Dosage Form
-
Strength
60MG/6ML (10MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DULOXETINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
DULOXETINE HYDROCHLORIDE
Application Number
90775
Product Number
1
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DULOXETINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
DULOXETINE HYDROCHLORIDE
Application Number
90775
Product Number
2
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
DULOXETINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
60MG
Approval Date
-
Active Ingredient
DULOXETINE HYDROCHLORIDE
Application Number
90775
Product Number
3
Dosage Form
-
Strength
60MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EPINASTINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
-
Active Ingredient
EPINASTINE HYDROCHLORIDE
Application Number
90950
Product Number
1
Dosage Form
-
Strength
0.05%
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ERELZI
Product Number
1
Dosage Form
-
Strength
25MG/0.5ML
Approval Date
-
Active Ingredient
ETANERCEPT-SZZS
Application Number
761042
Product Number
1
Dosage Form
-
Strength
25MG/0.5ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ERELZI
Product Number
2
Dosage Form
-
Strength
50MG/ML
Approval Date
-
Active Ingredient
ETANERCEPT-SZZS
Application Number
761042
Product Number
2
Dosage Form
-
Strength
50MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESCITALOPRAM OXALATE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
ESCITALOPRAM OXALATE
Application Number
78467
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESCITALOPRAM OXALATE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
ESCITALOPRAM OXALATE
Application Number
78467
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESCITALOPRAM OXALATE
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
ESCITALOPRAM OXALATE
Application Number
78467
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESTRADIOL
Product Number
1
Dosage Form
-
Strength
0.0375MG/24HR
Approval Date
-
Active Ingredient
ESTRADIOL
Application Number
20538
Product Number
1
Dosage Form
-
Strength
0.0375MG/24HR
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESTRADIOL
Product Number
2
Dosage Form
-
Strength
0.075MG/24HR
Approval Date
-
Active Ingredient
ESTRADIOL
Application Number
20538
Product Number
2
Dosage Form
-
Strength
0.075MG/24HR
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESTRADIOL
Product Number
3
Dosage Form
-
Strength
0.05MG/24HR
Approval Date
-
Active Ingredient
ESTRADIOL
Application Number
20538
Product Number
3
Dosage Form
-
Strength
0.05MG/24HR
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ESTRADIOL
Product Number
4
Dosage Form
-
Strength
0.1MG/24HR
Approval Date
-
Active Ingredient
ESTRADIOL
Application Number
20538
Product Number
4
Dosage Form
-
Strength
0.1MG/24HR
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FEXOFENADINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
FEXOFENADINE HYDROCHLORIDE
Application Number
76707
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FEXOFENADINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
60MG
Approval Date
-
Active Ingredient
FEXOFENADINE HYDROCHLORIDE
Application Number
76707
Product Number
2
Dosage Form
-
Strength
60MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FEXOFENADINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
180MG
Approval Date
-
Active Ingredient
FEXOFENADINE HYDROCHLORIDE
Application Number
76707
Product Number
3
Dosage Form
-
Strength
180MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FLUPHENAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
FLUPHENAZINE HYDROCHLORIDE
Application Number
89585
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
HALOPERIDOL
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
-
Active Ingredient
HALOPERIDOL
Application Number
71206
Product Number
1
Dosage Form
-
Strength
0.5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
HALOPERIDOL
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Active Ingredient
HALOPERIDOL
Application Number
71207
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
HALOPERIDOL
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Active Ingredient
HALOPERIDOL
Application Number
71208
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LORAZEPAM
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Active Ingredient
LORAZEPAM
Application Number
71404
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MINOCYCLINE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
EQ 65MG BASE
Approval Date
-
Active Ingredient
MINOCYCLINE HYDROCHLORIDE
Application Number
90422
Product Number
4
Dosage Form
-
Strength
EQ 65MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MINOCYCLINE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
EQ 115MG BASE
Approval Date
-
Active Ingredient
MINOCYCLINE HYDROCHLORIDE
Application Number
90422
Product Number
5
Dosage Form
-
Strength
EQ 115MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MINOCYCLINE HYDROCHLORIDE
Product Number
6
Dosage Form
-
Strength
EQ 55MG BASE
Approval Date
-
Active Ingredient
MINOCYCLINE HYDROCHLORIDE
Application Number
90422
Product Number
6
Dosage Form
-
Strength
EQ 55MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MINOCYCLINE HYDROCHLORIDE
Product Number
7
Dosage Form
-
Strength
EQ 80MG BASE
Approval Date
-
Active Ingredient
MINOCYCLINE HYDROCHLORIDE
Application Number
90422
Product Number
7
Dosage Form
-
Strength
EQ 80MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MINOCYCLINE HYDROCHLORIDE
Product Number
8
Dosage Form
-
Strength
EQ 105MG BASE
Approval Date
-
Active Ingredient
MINOCYCLINE HYDROCHLORIDE
Application Number
90422
Product Number
8
Dosage Form
-
Strength
EQ 105MG BASE
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MODAFINIL
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
MODAFINIL
Application Number
76935
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MODAFINIL
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Active Ingredient
MODAFINIL
Application Number
76935
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OLOPATADINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
-
Active Ingredient
OLOPATADINE HYDROCHLORIDE
Application Number
90972
Product Number
1
Dosage Form
-
Strength
0.1%
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OMEPRAZOLE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
OMEPRAZOLE
Application Number
75791
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OMEPRAZOLE
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
OMEPRAZOLE
Application Number
75791
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OMNITROPE
Product Number
1
Dosage Form
-
Strength
5.8MG/VIAL
Approval Date
-
Active Ingredient
SOMATROPIN
Application Number
21426
Product Number
1
Dosage Form
-
Strength
5.8MG/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OMNITROPE
Product Number
2
Dosage Form
-
Strength
1.5MG/VIAL
Approval Date
-
Active Ingredient
SOMATROPIN
Application Number
21426
Product Number
2
Dosage Form
-
Strength
1.5MG/VIAL
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OMNITROPE
Product Number
3
Dosage Form
-
Strength
5MG/1.5ML
Approval Date
-
Active Ingredient
SOMATROPIN
Application Number
21426
Product Number
3
Dosage Form
-
Strength
5MG/1.5ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
OMNITROPE
Product Number
4
Dosage Form
-
Strength
10MG/1.5ML
Approval Date
-
Active Ingredient
SOMATROPIN
Application Number
21426
Product Number
4
Dosage Form
-
Strength
10MG/1.5ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Active Ingredient
PERPHENAZINE
Application Number
89683
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
-
Active Ingredient
PERPHENAZINE
Application Number
89684
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PERPHENAZINE
Product Number
1
Dosage Form
-
Strength
16MG
Approval Date
-
Active Ingredient
PERPHENAZINE
Application Number
89686
Product Number
1
Dosage Form
-
Strength
16MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
-
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
87301
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
RECLAST
Product Number
1
Dosage Form
-
Strength
5MG/100ML
Approval Date
-
Active Ingredient
ZOLEDRONIC ACID
Application Number
22080
Product Number
1
Dosage Form
-
Strength
5MG/100ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ROSIGLITAZONE MALEATE
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Active Ingredient
ROSIGLITAZONE MALEATE
Application Number
78674
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ROSIGLITAZONE MALEATE
Product Number
2
Dosage Form
-
Strength
4MG
Approval Date
-
Active Ingredient
ROSIGLITAZONE MALEATE
Application Number
78674
Product Number
2
Dosage Form
-
Strength
4MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ROSIGLITAZONE MALEATE
Product Number
3
Dosage Form
-
Strength
8MG
Approval Date
-
Active Ingredient
ROSIGLITAZONE MALEATE
Application Number
78674
Product Number
3
Dosage Form
-
Strength
8MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
THIOTHIXENE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
THIOTHIXENE
Application Number
71530
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TOLTERODINE TARTRATE
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Active Ingredient
TOLTERODINE TARTRATE
Application Number
78419
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TOLTERODINE TARTRATE
Product Number
2
Dosage Form
-
Strength
2MG
Approval Date
-
Active Ingredient
TOLTERODINE TARTRATE
Application Number
78419
Product Number
2
Dosage Form
-
Strength
2MG
Approval Date
-
Regulatory Status
Unclassified
Drug Status Breakdown
50 total- Unclassified
Official Source
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Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Application Number
85970
Product Number
1
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Dosage Form
-
Strength
150MG
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