Ipca Laboratories Discontinued
FDA Approved Drugs

Ipca Laboratories Discontinued

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.

Discontinued
  • Total Records 36
  • Latest Approval Date May 29, 2024
  • Data Source FDA
  • First Approval Date Jul 20, 2007
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Discontinued
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Company Overview

Company

Ipca Laboratories Discontinued

Country

India

Website

Visit Website

Email

swapna.ugale@ipca.com

Social Profiles

LinkedIn
Company Snapshot

Ipca Laboratories Discontinued

Kandivli (West), Mumbai – 400 067, Maharashtra

India

www.ipca.com/ swapna.ugale@ipca.com View on Map
FDA Approved Drug Records ( 36 records )
2011
16 Mar
Discontinued Application: 90637

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2011-03-16

90637 / 1

Active Ingredient

ALLOPURINOL

Application Number

90637

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2011-03-16

Regulatory Status

Discontinued

2011
16 Mar
Discontinued Application: 90637

Drug Name

ALLOPURINOL

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2011-03-16

90637 / 2

Active Ingredient

ALLOPURINOL

Application Number

90637

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2011-03-16

Regulatory Status

Discontinued

2009
03 Dec
Discontinued Application: 90249

Drug Name

CHLOROQUINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2009-12-03

90249 / 1

Active Ingredient

CHLOROQUINE PHOSPHATE

Application Number

90249

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2009-12-03

Regulatory Status

Discontinued

2009
03 Dec
Discontinued Application: 90610

Drug Name

CHLOROQUINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2009-12-03

90610 / 1

Active Ingredient

CHLOROQUINE PHOSPHATE

Application Number

90610

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2009-12-03

Regulatory Status

Discontinued

2023
29 Dec
Discontinued Application: 206222

Drug Name

ESZOPICLONE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2023-12-29

206222 / 1

Active Ingredient

ESZOPICLONE

Application Number

206222

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2023-12-29

Regulatory Status

Discontinued

2023
29 Dec
Discontinued Application: 206222

Drug Name

ESZOPICLONE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2023-12-29

206222 / 2

Active Ingredient

ESZOPICLONE

Application Number

206222

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2023-12-29

Regulatory Status

Discontinued

2023
29 Dec
Discontinued Application: 206222

Drug Name

ESZOPICLONE

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

2023-12-29

206222 / 3

Active Ingredient

ESZOPICLONE

Application Number

206222

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

2023-12-29

Regulatory Status

Discontinued

2023
20 Nov
Discontinued Application: 208928

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2023-11-20

208928 / 1

Active Ingredient

GABAPENTIN

Application Number

208928

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2023-11-20

Regulatory Status

Discontinued

2023
20 Nov
Discontinued Application: 208928

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2023-11-20

208928 / 2

Active Ingredient

GABAPENTIN

Application Number

208928

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2023-11-20

Regulatory Status

Discontinued

2023
20 Nov
Discontinued Application: 208928

Drug Name

GABAPENTIN

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2023-11-20

208928 / 3

Active Ingredient

GABAPENTIN

Application Number

208928

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2023-11-20

Regulatory Status

Discontinued

2024
29 May
Discontinued Application: 209855

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2024-05-29

209855 / 1

Active Ingredient

GABAPENTIN

Application Number

209855

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2024-05-29

Regulatory Status

Discontinued

2024
29 May
Discontinued Application: 209855

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

2024-05-29

209855 / 2

Active Ingredient

GABAPENTIN

Application Number

209855

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

2024-05-29

Regulatory Status

Discontinued

2007
20 Jul
Discontinued Application: 40807

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2007-07-20

40807 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40807

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2007-07-20

Regulatory Status

Discontinued

2007
20 Jul
Discontinued Application: 40807

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2007-07-20

40807 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40807

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2007-07-20

Regulatory Status

Discontinued

2007
20 Jul
Discontinued Application: 40807

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2007-07-20

40807 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40807

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2007-07-20

Regulatory Status

Discontinued

2009
02 Apr
Discontinued Application: 79237

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2009-04-02

79237 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

79237

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2009-04-02

Regulatory Status

Discontinued

2024
22 May
Discontinued Application: 211056

Drug Name

IRBESARTAN

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2024-05-22

211056 / 1

Active Ingredient

IRBESARTAN

Application Number

211056

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2024-05-22

Regulatory Status

Discontinued

2024
22 May
Discontinued Application: 211056

Drug Name

IRBESARTAN

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2024-05-22

211056 / 2

Active Ingredient

IRBESARTAN

Application Number

211056

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2024-05-22

Regulatory Status

Discontinued

2024
22 May
Discontinued Application: 211056

Drug Name

IRBESARTAN

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2024-05-22

211056 / 3

Active Ingredient

IRBESARTAN

Application Number

211056

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2024-05-22

Regulatory Status

Discontinued

2024
06 May
Discontinued Application: 204626

Drug Name

LEVOCETIRIZINE DIHYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2024-05-06

204626 / 1

Active Ingredient

LEVOCETIRIZINE DIHYDROCHLORIDE

Application Number

204626

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2024-05-06

Regulatory Status

Discontinued

2013
30 Aug
Discontinued Application: 200290

Drug Name

LOSARTAN POTASSIUM

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2013-08-30

200290 / 1

Active Ingredient

LOSARTAN POTASSIUM

Application Number

200290

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2013-08-30

Regulatory Status

Discontinued

2013
30 Aug
Discontinued Application: 200290

Drug Name

LOSARTAN POTASSIUM

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2013-08-30

200290 / 2

Active Ingredient

LOSARTAN POTASSIUM

Application Number

200290

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2013-08-30

Regulatory Status

Discontinued

2013
30 Aug
Discontinued Application: 200290

Drug Name

LOSARTAN POTASSIUM

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2013-08-30

200290 / 3

Active Ingredient

LOSARTAN POTASSIUM

Application Number

200290

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2013-08-30

Regulatory Status

Discontinued

2013
01 Mar
Discontinued Application: 201682

Drug Name

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;50MG

Approval Date

2013-03-01

201682 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM

Application Number

201682

Product Number

1

Dosage Form

-

Strength

12.5MG;50MG

Approval Date

2013-03-01

Regulatory Status

Discontinued

2013
01 Mar
Discontinued Application: 201682

Drug Name

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;100MG

Approval Date

2013-03-01

201682 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM

Application Number

201682

Product Number

2

Dosage Form

-

Strength

12.5MG;100MG

Approval Date

2013-03-01

Regulatory Status

Discontinued

2013
01 Mar
Discontinued Application: 201682

Drug Name

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

25MG;100MG

Approval Date

2013-03-01

201682 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM

Application Number

201682

Product Number

3

Dosage Form

-

Strength

25MG;100MG

Approval Date

2013-03-01

Regulatory Status

Discontinued

2007
06 Aug
Discontinued Application: 78422

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2007-08-06

78422 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

78422

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2007-08-06

Regulatory Status

Discontinued

2007
06 Aug
Discontinued Application: 78422

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2007-08-06

78422 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

78422

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2007-08-06

Regulatory Status

Discontinued

2007
06 Aug
Discontinued Application: 78422

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2007-08-06

78422 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

78422

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2007-08-06

Regulatory Status

Discontinued

2024
20 May
Discontinued Application: 205983

Drug Name

QUETIAPINE FUMARATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2024-05-20

205983 / 1

Active Ingredient

QUETIAPINE FUMARATE

Application Number

205983

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2024-05-20

Regulatory Status

Discontinued

2024
20 May
Discontinued Application: 205983

Drug Name

QUETIAPINE FUMARATE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2024-05-20

205983 / 2

Active Ingredient

QUETIAPINE FUMARATE

Application Number

205983

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2024-05-20

Regulatory Status

Discontinued

2024
20 May
Discontinued Application: 205983

Drug Name

QUETIAPINE FUMARATE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2024-05-20

205983 / 3

Active Ingredient

QUETIAPINE FUMARATE

Application Number

205983

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2024-05-20

Regulatory Status

Discontinued

2024
20 May
Discontinued Application: 205983

Drug Name

QUETIAPINE FUMARATE

Product Number

4

Dosage Form

-

Strength

EQ 200MG BASE

Approval Date

2024-05-20

205983 / 4

Active Ingredient

QUETIAPINE FUMARATE

Application Number

205983

Product Number

4

Dosage Form

-

Strength

EQ 200MG BASE

Approval Date

2024-05-20

Regulatory Status

Discontinued

2024
20 May
Discontinued Application: 205983

Drug Name

QUETIAPINE FUMARATE

Product Number

5

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2024-05-20

205983 / 5

Active Ingredient

QUETIAPINE FUMARATE

Application Number

205983

Product Number

5

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2024-05-20

Regulatory Status

Discontinued

2024
20 May
Discontinued Application: 205983

Drug Name

QUETIAPINE FUMARATE

Product Number

6

Dosage Form

-

Strength

EQ 400MG BASE

Approval Date

2024-05-20

205983 / 6

Active Ingredient

QUETIAPINE FUMARATE

Application Number

205983

Product Number

6

Dosage Form

-

Strength

EQ 400MG BASE

Approval Date

2024-05-20

Regulatory Status

Discontinued

2012
16 Nov
Discontinued Application: 201973

Drug Name

TRAMADOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2012-11-16

201973 / 1

Active Ingredient

TRAMADOL HYDROCHLORIDE

Application Number

201973

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2012-11-16

Regulatory Status

Discontinued

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Drug Status Breakdown
36 total
  • 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

ALLOPURINOL

Application Number

90637

Product Number

1

Active Ingredient

ALLOPURINOL

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

Approved drug product information

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