INDICUS PHARMA
FDA Approved Drugs

INDICUS PHARMA

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.

RX Discontinued
  • Total Records 7
  • Latest Approval Date Jun 13, 2012
  • Data Source FDA
  • First Approval Date Nov 25, 2008
All
7
View
Discontinued
6
View
RX
1
View
Company Overview

Company

INDICUS PHARMA

Country

U.S.A

Website

Social Profiles

Company Snapshot

INDICUS PHARMA

Dr. Nitin Sheth, PH.D President & CEO

U.S.A

nitin@indicuspharma.com View on Map
FDA Approved Drug Records ( 7 records )
2011
14 Jul
RX Application: 90779

Drug Name

ACETAZOLAMIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2011-07-14

90779 / 1

Active Ingredient

ACETAZOLAMIDE

Application Number

90779

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2011-07-14

Regulatory Status

RX

2012
13 Jun
Discontinued Application: 201634

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2012-06-13

201634 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

201634

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2012-06-13

Regulatory Status

Discontinued

2012
13 Jun
Discontinued Application: 201634

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2012-06-13

201634 / 2

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

201634

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2012-06-13

Regulatory Status

Discontinued

2011
03 Jun
Discontinued Application: 201804

Drug Name

LETROZOLE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2011-06-03

201804 / 1

Active Ingredient

LETROZOLE

Application Number

201804

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2011-06-03

Regulatory Status

Discontinued

2008
25 Nov
Discontinued Application: 79148

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2008-11-25

79148 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

79148

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2008-11-25

Regulatory Status

Discontinued

2008
25 Nov
Discontinued Application: 79148

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2008-11-25

79148 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

79148

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2008-11-25

Regulatory Status

Discontinued

2008
25 Nov
Discontinued Application: 79148

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2008-11-25

79148 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

79148

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2008-11-25

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • RX
  • Discontinued
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

ACETAZOLAMIDE

Application Number

90779

Product Number

1

Active Ingredient

ACETAZOLAMIDE

Dosage Form

-

Strength

500MG

FDA Approved Drug Data

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