Barr Laboratories Inc. Unclassified
FDA Approved Drugs
Barr Laboratories Inc. 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 16
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
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Barr Laboratories Inc. Unclassified
225 Summit Ave, Montvale, NJ 07645
U.S.A
www.barrlabs.com View on MapFDA Approved Drug Records ( 16 records )
Drug Name
ARIPIPRAZOLE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78612
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
2
Dosage Form
-
Strength
15MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78612
Product Number
2
Dosage Form
-
Strength
15MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78612
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
4
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78612
Product Number
4
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78613
Product Number
1
Dosage Form
-
Strength
2MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78613
Product Number
2
Dosage Form
-
Strength
5MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
3
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78613
Product Number
3
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
4
Dosage Form
-
Strength
15MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78613
Product Number
4
Dosage Form
-
Strength
15MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
5
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78613
Product Number
5
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ARIPIPRAZOLE
Product Number
6
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
ARIPIPRAZOLE
Application Number
78613
Product Number
6
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CINACALCET HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
-
Active Ingredient
CINACALCET HYDROCHLORIDE
Application Number
90476
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CINACALCET HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
60MG
Approval Date
-
Active Ingredient
CINACALCET HYDROCHLORIDE
Application Number
90476
Product Number
2
Dosage Form
-
Strength
60MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CINACALCET HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
90MG
Approval Date
-
Active Ingredient
CINACALCET HYDROCHLORIDE
Application Number
90476
Product Number
3
Dosage Form
-
Strength
90MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
MODAFINIL
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
MODAFINIL
Application Number
76597
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
76597
Product Number
2
Dosage Form
-
Strength
200MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ZIDOVUDINE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
ZIDOVUDINE
Application Number
74047
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Status Breakdown
16 total- Unclassified
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
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Explore important FDA approved drug information available in the records above.
Drug Name
ARIPIPRAZOLE
Application Number
78612
Product Number
1
Active Ingredient
ARIPIPRAZOLE
Dosage Form
-
Strength
10MG
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