Jubilant Cadista Pharmaceuticals Inc. Discontinued
FDA Approved Drugs

Jubilant Cadista Pharmaceuticals Inc. 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 19
  • Latest Approval Date Apr 25, 2019
  • Data Source FDA
  • First Approval Date Feb 01, 1988
All
73
View
Discontinued
19
View
RX
54
View
Company Overview

Company

Jubilant Cadista Pharmaceuticals Inc. Discontinued

Country

U.S.A

Website

Visit Website

Email

customer.service@cadista.com

Social Profiles

Company Snapshot

Jubilant Cadista Pharmaceuticals Inc. Discontinued

207, Kiley Drive, Salisbury, Maryland-21801, USA

U.S.A

www.cadista.com/ customer.service@cadista.com View on Map
FDA Approved Drug Records ( 19 records )
2010
18 Feb
Discontinued Application: 90557

Drug Name

ALENDRONATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2010-02-18

90557 / 1

Active Ingredient

ALENDRONATE SODIUM

Application Number

90557

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2010-02-18

Regulatory Status

Discontinued

2010
18 Feb
Discontinued Application: 90557

Drug Name

ALENDRONATE SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2010-02-18

90557 / 2

Active Ingredient

ALENDRONATE SODIUM

Application Number

90557

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2010-02-18

Regulatory Status

Discontinued

2010
18 Feb
Discontinued Application: 90557

Drug Name

ALENDRONATE SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 35MG BASE

Approval Date

2010-02-18

90557 / 3

Active Ingredient

ALENDRONATE SODIUM

Application Number

90557

Product Number

3

Dosage Form

-

Strength

EQ 35MG BASE

Approval Date

2010-02-18

Regulatory Status

Discontinued

2010
18 Feb
Discontinued Application: 90557

Drug Name

ALENDRONATE SODIUM

Product Number

4

Dosage Form

-

Strength

EQ 70MG BASE

Approval Date

2010-02-18

90557 / 4

Active Ingredient

ALENDRONATE SODIUM

Application Number

90557

Product Number

4

Dosage Form

-

Strength

EQ 70MG BASE

Approval Date

2010-02-18

Regulatory Status

Discontinued

1988
01 Feb
Discontinued Application: 71940

Drug Name

CARBAMAZEPINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1988-02-01

71940 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

71940

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1988-02-01

Regulatory Status

Discontinued

2019
25 Apr
Discontinued Application: 206714

Drug Name

CLARITHROMYCIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2019-04-25

206714 / 1

Active Ingredient

CLARITHROMYCIN

Application Number

206714

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2019-04-25

Regulatory Status

Discontinued

2019
25 Apr
Discontinued Application: 206714

Drug Name

CLARITHROMYCIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2019-04-25

206714 / 2

Active Ingredient

CLARITHROMYCIN

Application Number

206714

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2019-04-25

Regulatory Status

Discontinued

2017
22 Dec
Discontinued Application: 209423

Drug Name

DROSPIRENONE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

3MG;0.02MG

Approval Date

2017-12-22

209423 / 1

Active Ingredient

DROSPIRENONE; ETHINYL ESTRADIOL

Application Number

209423

Product Number

1

Dosage Form

-

Strength

3MG;0.02MG

Approval Date

2017-12-22

Regulatory Status

Discontinued

2018
10 Sep
Discontinued Application: 210017

Drug Name

DROSPIRENONE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

3MG;0.03MG

Approval Date

2018-09-10

210017 / 1

Active Ingredient

DROSPIRENONE; ETHINYL ESTRADIOL

Application Number

210017

Product Number

1

Dosage Form

-

Strength

3MG;0.03MG

Approval Date

2018-09-10

Regulatory Status

Discontinued

2005
14 Jun
Discontinued Application: 40514

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2005-06-14

40514 / 1

Active Ingredient

FOLIC ACID

Application Number

40514

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2005-06-14

Regulatory Status

Discontinued

2007
04 Sep
Discontinued Application: 40809

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2007-09-04

40809 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40809

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2007-09-04

Regulatory Status

Discontinued

2007
04 Sep
Discontinued Application: 40809

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2007-09-04

40809 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40809

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2007-09-04

Regulatory Status

Discontinued

2014
15 Dec
Discontinued Application: 90661

Drug Name

MYCOPHENOLATE MOFETIL

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2014-12-15

90661 / 1

Active Ingredient

MYCOPHENOLATE MOFETIL

Application Number

90661

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2014-12-15

Regulatory Status

Discontinued

2014
15 Dec
Discontinued Application: 90762

Drug Name

MYCOPHENOLATE MOFETIL

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2014-12-15

90762 / 1

Active Ingredient

MYCOPHENOLATE MOFETIL

Application Number

90762

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2014-12-15

Regulatory Status

Discontinued

2010
25 Jan
Discontinued Application: 90239

Drug Name

OXCARBAZEPINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2010-01-25

90239 / 1

Active Ingredient

OXCARBAZEPINE

Application Number

90239

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2010-01-25

Regulatory Status

Discontinued

2010
25 Jan
Discontinued Application: 90239

Drug Name

OXCARBAZEPINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2010-01-25

90239 / 2

Active Ingredient

OXCARBAZEPINE

Application Number

90239

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2010-01-25

Regulatory Status

Discontinued

2010
25 Jan
Discontinued Application: 90239

Drug Name

OXCARBAZEPINE

Product Number

3

Dosage Form

-

Strength

600MG

Approval Date

2010-01-25

90239 / 3

Active Ingredient

OXCARBAZEPINE

Application Number

90239

Product Number

3

Dosage Form

-

Strength

600MG

Approval Date

2010-01-25

Regulatory Status

Discontinued

2016
18 May
Discontinued Application: 203352

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

2016-05-18

203352 / 1

Active Ingredient

SODIUM CHLORIDE

Application Number

203352

Product Number

1

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

2016-05-18

Regulatory Status

Discontinued

2016
18 May
Discontinued Application: 203352

Drug Name

SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

27MG/3ML (9MG/ML)

Approval Date

2016-05-18

203352 / 2

Active Ingredient

SODIUM CHLORIDE

Application Number

203352

Product Number

2

Dosage Form

-

Strength

27MG/3ML (9MG/ML)

Approval Date

2016-05-18

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    1 View
  • FDA Approved Drugs Database
    73 View
Drug Status Breakdown
19 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

ALENDRONATE SODIUM

Application Number

90557

Product Number

1

Active Ingredient

ALENDRONATE SODIUM

Dosage Form

-

Strength

EQ 5MG BASE

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.
Login to Submit