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.

Unclassified
  • Total Records 16
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
269
View
Unclassified
16
View
Discontinued
165
View
OTC
1
View
RX
87
View
Company Overview

Company

Barr Laboratories Inc. Unclassified

Country

U.S.A

Email

Social Profiles

Company Snapshot

Barr Laboratories Inc. Unclassified

225 Summit Ave, Montvale, NJ 07645

U.S.A

www.barrlabs.com View on Map
FDA Approved Drug Records ( 16 records )
-
Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

78612 / 1

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

-

78612 / 2

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

-

78612 / 3

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78612

Drug Name

ARIPIPRAZOLE

Product Number

4

Dosage Form

-

Strength

30MG

Approval Date

-

78612 / 4

Active Ingredient

ARIPIPRAZOLE

Application Number

78612

Product Number

4

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

78613 / 1

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

78613 / 2

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

-

78613 / 3

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

-

78613 / 4

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

-

78613 / 5

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78613

Drug Name

ARIPIPRAZOLE

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

-

78613 / 6

Active Ingredient

ARIPIPRAZOLE

Application Number

78613

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90476

Drug Name

CINACALCET HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

-

90476 / 1

Active Ingredient

CINACALCET HYDROCHLORIDE

Application Number

90476

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90476

Drug Name

CINACALCET HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

-

90476 / 2

Active Ingredient

CINACALCET HYDROCHLORIDE

Application Number

90476

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90476

Drug Name

CINACALCET HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

-

90476 / 3

Active Ingredient

CINACALCET HYDROCHLORIDE

Application Number

90476

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76597

Drug Name

MODAFINIL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

76597 / 1

Active Ingredient

MODAFINIL

Application Number

76597

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76597

Drug Name

MODAFINIL

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

76597 / 2

Active Ingredient

MODAFINIL

Application Number

76597

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 74047

Drug Name

ZIDOVUDINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

74047 / 1

Active Ingredient

ZIDOVUDINE

Application Number

74047

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

Related Databases
  • FDA Inspections
    13 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    269 View
  • Drug Prices in Switzerland
    0 View
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.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.