Jubilant Generics Discontinued
FDA Approved Drugs

Jubilant Generics 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 50
  • Latest Approval Date May 14, 2018
  • Data Source FDA
  • First Approval Date Feb 28, 2011
All
132
View
Unclassified
1
View
Discontinued
50
View
OTC
4
View
RX
77
View
Company Overview

Company

Jubilant Generics Discontinued

Country

India

Website

Visit Website

Email

support@jubl.com

Social Profiles

Company Snapshot

Jubilant Generics Discontinued

Bhartiagram Gajraula, Distt. Amroha - 244223, Uttar Pradesh, India

India

www.jubilantgenerics.com/ support@jubl.com View on Map
FDA Approved Drug Records ( 50 records )
2018
07 Feb
Discontinued Application: 210403

Drug Name

AMANTADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2018-02-07

210403 / 1

Active Ingredient

AMANTADINE HYDROCHLORIDE

Application Number

210403

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2018-02-07

Regulatory Status

Discontinued

2017
15 May
Discontinued Application: 207450

Drug Name

AMLODIPINE AND OLMESARTAN MEDOXOMIL

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE;20MG

Approval Date

2017-05-15

207450 / 1

Active Ingredient

AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL

Application Number

207450

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE;20MG

Approval Date

2017-05-15

Regulatory Status

Discontinued

2017
15 May
Discontinued Application: 207450

Drug Name

AMLODIPINE AND OLMESARTAN MEDOXOMIL

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE;40MG

Approval Date

2017-05-15

207450 / 2

Active Ingredient

AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL

Application Number

207450

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE;40MG

Approval Date

2017-05-15

Regulatory Status

Discontinued

2017
15 May
Discontinued Application: 207450

Drug Name

AMLODIPINE AND OLMESARTAN MEDOXOMIL

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE;20MG

Approval Date

2017-05-15

207450 / 3

Active Ingredient

AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL

Application Number

207450

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE;20MG

Approval Date

2017-05-15

Regulatory Status

Discontinued

2017
15 May
Discontinued Application: 207450

Drug Name

AMLODIPINE AND OLMESARTAN MEDOXOMIL

Product Number

4

Dosage Form

-

Strength

EQ 10MG BASE;40MG

Approval Date

2017-05-15

207450 / 4

Active Ingredient

AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL

Application Number

207450

Product Number

4

Dosage Form

-

Strength

EQ 10MG BASE;40MG

Approval Date

2017-05-15

Regulatory Status

Discontinued

2013
11 Oct
Discontinued Application: 202774

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2013-10-11

202774 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

202774

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2013-10-11

Regulatory Status

Discontinued

2013
11 Oct
Discontinued Application: 202774

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2013-10-11

202774 / 2

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

202774

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2013-10-11

Regulatory Status

Discontinued

2013
11 Oct
Discontinued Application: 202774

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2013-10-11

202774 / 3

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

202774

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2013-10-11

Regulatory Status

Discontinued

2013
11 Oct
Discontinued Application: 202775

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2013-10-11

202775 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

202775

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2013-10-11

Regulatory Status

Discontinued

2017
30 Jun
Discontinued Application: 207459

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2017-06-30

207459 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

207459

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2017-06-30

Regulatory Status

Discontinued

2017
30 Jun
Discontinued Application: 207459

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2017-06-30

207459 / 2

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

207459

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2017-06-30

Regulatory Status

Discontinued

2017
04 Apr
Discontinued Application: 207061

Drug Name

CELECOXIB

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2017-04-04

207061 / 1

Active Ingredient

CELECOXIB

Application Number

207061

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2017-04-04

Regulatory Status

Discontinued

2017
04 Apr
Discontinued Application: 207061

Drug Name

CELECOXIB

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2017-04-04

207061 / 2

Active Ingredient

CELECOXIB

Application Number

207061

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2017-04-04

Regulatory Status

Discontinued

2017
04 Apr
Discontinued Application: 207061

Drug Name

CELECOXIB

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2017-04-04

207061 / 3

Active Ingredient

CELECOXIB

Application Number

207061

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2017-04-04

Regulatory Status

Discontinued

2017
04 Apr
Discontinued Application: 207061

Drug Name

CELECOXIB

Product Number

4

Dosage Form

-

Strength

400MG

Approval Date

2017-04-04

207061 / 4

Active Ingredient

CELECOXIB

Application Number

207061

Product Number

4

Dosage Form

-

Strength

400MG

Approval Date

2017-04-04

Regulatory Status

Discontinued

2015
23 Dec
Discontinued Application: 205407

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-12-23

205407 / 1

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

205407

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-12-23

Regulatory Status

Discontinued

2015
23 Dec
Discontinued Application: 205407

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2015-12-23

205407 / 2

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

205407

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2015-12-23

Regulatory Status

Discontinued

2015
23 Dec
Discontinued Application: 205407

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2015-12-23

205407 / 3

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

205407

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2015-12-23

Regulatory Status

Discontinued

2016
12 Oct
Discontinued Application: 205550

Drug Name

DARIFENACIN HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 7.5MG BASE

Approval Date

2016-10-12

205550 / 1

Active Ingredient

DARIFENACIN HYDROBROMIDE

Application Number

205550

Product Number

1

Dosage Form

-

Strength

EQ 7.5MG BASE

Approval Date

2016-10-12

Regulatory Status

Discontinued

2016
12 Oct
Discontinued Application: 205550

Drug Name

DARIFENACIN HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2016-10-12

205550 / 2

Active Ingredient

DARIFENACIN HYDROBROMIDE

Application Number

205550

Product Number

2

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2016-10-12

Regulatory Status

Discontinued

2016
19 Aug
Discontinued Application: 203983

Drug Name

FELODIPINE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2016-08-19

203983 / 1

Active Ingredient

FELODIPINE

Application Number

203983

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2016-08-19

Regulatory Status

Discontinued

2016
19 Aug
Discontinued Application: 203983

Drug Name

FELODIPINE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2016-08-19

203983 / 2

Active Ingredient

FELODIPINE

Application Number

203983

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2016-08-19

Regulatory Status

Discontinued

2016
19 Aug
Discontinued Application: 203983

Drug Name

FELODIPINE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2016-08-19

203983 / 3

Active Ingredient

FELODIPINE

Application Number

203983

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2016-08-19

Regulatory Status

Discontinued

2015
05 Oct
Discontinued Application: 202706

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2015-10-05

202706 / 1

Active Ingredient

INDOMETHACIN

Application Number

202706

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2015-10-05

Regulatory Status

Discontinued

2017
25 Aug
Discontinued Application: 205215

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2017-08-25

205215 / 1

Active Ingredient

INDOMETHACIN

Application Number

205215

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2017-08-25

Regulatory Status

Discontinued

2017
25 Aug
Discontinued Application: 205215

Drug Name

INDOMETHACIN

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2017-08-25

205215 / 2

Active Ingredient

INDOMETHACIN

Application Number

205215

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2017-08-25

Regulatory Status

Discontinued

2017
23 Feb
Discontinued Application: 203445

Drug Name

ITRACONAZOLE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2017-02-23

203445 / 1

Active Ingredient

ITRACONAZOLE

Application Number

203445

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2017-02-23

Regulatory Status

Discontinued

2011
28 Feb
Discontinued Application: 200220

Drug Name

LAMOTRIGINE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-02-28

200220 / 1

Active Ingredient

LAMOTRIGINE

Application Number

200220

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-02-28

Regulatory Status

Discontinued

2011
28 Feb
Discontinued Application: 200220

Drug Name

LAMOTRIGINE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2011-02-28

200220 / 2

Active Ingredient

LAMOTRIGINE

Application Number

200220

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2011-02-28

Regulatory Status

Discontinued

2016
02 Jun
Discontinued Application: 206838

Drug Name

LEVETIRACETAM

Product Number

1

Dosage Form

-

Strength

500MG/5ML (100MG/ML)

Approval Date

2016-06-02

206838 / 1

Active Ingredient

LEVETIRACETAM

Application Number

206838

Product Number

1

Dosage Form

-

Strength

500MG/5ML (100MG/ML)

Approval Date

2016-06-02

Regulatory Status

Discontinued

2015
19 Jun
Discontinued Application: 203613

Drug Name

LEVOFLOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2015-06-19

203613 / 1

Active Ingredient

LEVOFLOXACIN

Application Number

203613

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2015-06-19

Regulatory Status

Discontinued

2015
19 Jun
Discontinued Application: 203613

Drug Name

LEVOFLOXACIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2015-06-19

203613 / 2

Active Ingredient

LEVOFLOXACIN

Application Number

203613

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2015-06-19

Regulatory Status

Discontinued

2015
13 Oct
Discontinued Application: 91585

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2015-10-13

91585 / 1

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

91585

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2015-10-13

Regulatory Status

Discontinued

2015
13 Oct
Discontinued Application: 91585

Drug Name

MEMANTINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2015-10-13

91585 / 2

Active Ingredient

MEMANTINE HYDROCHLORIDE

Application Number

91585

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2015-10-13

Regulatory Status

Discontinued

2015
27 Feb
Discontinued Application: 203795

Drug Name

MONTELUKAST SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2015-02-27

203795 / 1

Active Ingredient

MONTELUKAST SODIUM

Application Number

203795

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2015-02-27

Regulatory Status

Discontinued

2015
27 Feb
Discontinued Application: 203795

Drug Name

MONTELUKAST SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-02-27

203795 / 2

Active Ingredient

MONTELUKAST SODIUM

Application Number

203795

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-02-27

Regulatory Status

Discontinued

2018
14 May
Discontinued Application: 209156

Drug Name

NIACIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2018-05-14

209156 / 1

Active Ingredient

NIACIN

Application Number

209156

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2018-05-14

Regulatory Status

Discontinued

2018
14 May
Discontinued Application: 209156

Drug Name

NIACIN

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2018-05-14

209156 / 2

Active Ingredient

NIACIN

Application Number

209156

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2018-05-14

Regulatory Status

Discontinued

2018
14 May
Discontinued Application: 209156

Drug Name

NIACIN

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2018-05-14

209156 / 3

Active Ingredient

NIACIN

Application Number

209156

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2018-05-14

Regulatory Status

Discontinued

2011
30 Aug
Discontinued Application: 90901

Drug Name

PANTOPRAZOLE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2011-08-30

90901 / 1

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

90901

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2011-08-30

Regulatory Status

Discontinued

2011
30 Aug
Discontinued Application: 90901

Drug Name

PANTOPRAZOLE SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2011-08-30

90901 / 2

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

90901

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2011-08-30

Regulatory Status

Discontinued

2015
27 Nov
Discontinued Application: 205528

Drug Name

PAROXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-11-27

205528 / 1

Active Ingredient

PAROXETINE HYDROCHLORIDE

Application Number

205528

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-11-27

Regulatory Status

Discontinued

2015
27 Nov
Discontinued Application: 205528

Drug Name

PAROXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2015-11-27

205528 / 2

Active Ingredient

PAROXETINE HYDROCHLORIDE

Application Number

205528

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2015-11-27

Regulatory Status

Discontinued

2015
27 Nov
Discontinued Application: 205528

Drug Name

PAROXETINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2015-11-27

205528 / 3

Active Ingredient

PAROXETINE HYDROCHLORIDE

Application Number

205528

Product Number

3

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2015-11-27

Regulatory Status

Discontinued

2015
27 Nov
Discontinued Application: 205528

Drug Name

PAROXETINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2015-11-27

205528 / 4

Active Ingredient

PAROXETINE HYDROCHLORIDE

Application Number

205528

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2015-11-27

Regulatory Status

Discontinued

2013
26 Nov
Discontinued Application: 203150

Drug Name

QUETIAPINE FUMARATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2013-11-26

203150 / 1

Active Ingredient

QUETIAPINE FUMARATE

Application Number

203150

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2013-11-26

Regulatory Status

Discontinued

2014
31 Dec
Discontinued Application: 203252

Drug Name

RIZATRIPTAN BENZOATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2014-12-31

203252 / 1

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

203252

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2014-12-31

Regulatory Status

Discontinued

2014
31 Dec
Discontinued Application: 203252

Drug Name

RIZATRIPTAN BENZOATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2014-12-31

203252 / 2

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

203252

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2014-12-31

Regulatory Status

Discontinued

2015
16 Oct
Discontinued Application: 203334

Drug Name

RIZATRIPTAN BENZOATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-10-16

203334 / 1

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

203334

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-10-16

Regulatory Status

Discontinued

2015
16 Oct
Discontinued Application: 203334

Drug Name

RIZATRIPTAN BENZOATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-10-16

203334 / 2

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

203334

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-10-16

Regulatory Status

Discontinued

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Drug Status Breakdown
50 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

AMANTADINE HYDROCHLORIDE

Application Number

210403

Product Number

1

Active Ingredient

AMANTADINE HYDROCHLORIDE

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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