Vista Pharmaceuticals
FDA Approved Drugs

Vista Pharmaceuticals

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 RX
  • Total Records 27
  • Latest Approval Date Aug 19, 2022
  • Data Source FDA
  • First Approval Date Sep 30, 1992
All
27
View
Discontinued
16
View
RX
11
View
Company Overview

Company

Vista Pharmaceuticals

Country

India

Website

Visit Website

Email

admin.hyd@vistapharmaceuticals.com

Social Profiles

Company Snapshot

Vista Pharmaceuticals

7-1-212/A/70, Plot # 85Shivbagh, AmeerpetHyderabad-500 016, Andhra Pradesh

India

vistapharmaceuticals.com/ admin.hyd@vistapharmaceuticals.com View on Map
FDA Approved Drug Records ( 27 records )
2021
11 Jan
Discontinued Application: 213951

Drug Name

ACYCLOVIR

Product Number

1

Dosage Form

-

Strength

200MG/5ML

Approval Date

2021-01-11

213951 / 1

Active Ingredient

ACYCLOVIR

Application Number

213951

Product Number

1

Dosage Form

-

Strength

200MG/5ML

Approval Date

2021-01-11

Regulatory Status

Discontinued

2020
26 Feb
Discontinued Application: 212814

Drug Name

AMINOCAPROIC ACID

Product Number

1

Dosage Form

-

Strength

0.25GM/ML

Approval Date

2020-02-26

212814 / 1

Active Ingredient

AMINOCAPROIC ACID

Application Number

212814

Product Number

1

Dosage Form

-

Strength

0.25GM/ML

Approval Date

2020-02-26

Regulatory Status

Discontinued

2019
26 Dec
RX Application: 212870

Drug Name

ARIPIPRAZOLE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2019-12-26

212870 / 1

Active Ingredient

ARIPIPRAZOLE

Application Number

212870

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2019-12-26

Regulatory Status

RX

2019
10 Jul
Discontinued Application: 210746

Drug Name

CLOBAZAM

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

2019-07-10

210746 / 1

Active Ingredient

CLOBAZAM

Application Number

210746

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

2019-07-10

Regulatory Status

Discontinued

2019
04 Oct
RX Application: 213000

Drug Name

DIGOXIN

Product Number

1

Dosage Form

-

Strength

0.05MG/ML

Approval Date

2019-10-04

213000 / 1

Active Ingredient

DIGOXIN

Application Number

213000

Product Number

1

Dosage Form

-

Strength

0.05MG/ML

Approval Date

2019-10-04

Regulatory Status

RX

1992
30 Sep
Discontinued Application: 74138

Drug Name

LACTULOSE

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1992-09-30

74138 / 1

Active Ingredient

LACTULOSE

Application Number

74138

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1992-09-30

Regulatory Status

Discontinued

2022
19 Aug
RX Application: 212677

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG/5ML

Approval Date

2022-08-19

212677 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

212677

Product Number

1

Dosage Form

-

Strength

500MG/5ML

Approval Date

2022-08-19

Regulatory Status

RX

1994
30 Nov
RX Application: 40088

Drug Name

METHADONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1994-11-30

40088 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

40088

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1994-11-30

Regulatory Status

RX

1998
29 May
Discontinued Application: 40241

Drug Name

METHADONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1998-05-29

40241 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

40241

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1998-05-29

Regulatory Status

Discontinued

1998
29 May
Discontinued Application: 40241

Drug Name

METHADONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1998-05-29

40241 / 2

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

40241

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1998-05-29

Regulatory Status

Discontinued

1998
25 Mar
RX Application: 75082

Drug Name

METHADONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1998-03-25

75082 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

75082

Product Number

1

Dosage Form

-

Strength

40MG

Approval Date

1998-03-25

Regulatory Status

RX

2010
30 Jun
RX Application: 90707

Drug Name

METHADONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2010-06-30

90707 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

90707

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2010-06-30

Regulatory Status

RX

2010
30 Jun
Discontinued Application: 90707

Drug Name

METHADONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG/5ML

Approval Date

2010-06-30

90707 / 2

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

90707

Product Number

2

Dosage Form

-

Strength

10MG/5ML

Approval Date

2010-06-30

Regulatory Status

Discontinued

2020
16 Mar
RX Application: 204166

Drug Name

METHADONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2020-03-16

204166 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

204166

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2020-03-16

Regulatory Status

RX

2001
26 Jan
Discontinued Application: 75051

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

2001-01-26

75051 / 1

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

75051

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

2001-01-26

Regulatory Status

Discontinued

2012
05 Jan
Discontinued Application: 201947

Drug Name

MORPHINE SULFATE

Product Number

1

Dosage Form

-

Strength

10MG/5ML

Approval Date

2012-01-05

201947 / 1

Active Ingredient

MORPHINE SULFATE

Application Number

201947

Product Number

1

Dosage Form

-

Strength

10MG/5ML

Approval Date

2012-01-05

Regulatory Status

Discontinued

2012
05 Jan
Discontinued Application: 201947

Drug Name

MORPHINE SULFATE

Product Number

2

Dosage Form

-

Strength

20MG/5ML

Approval Date

2012-01-05

201947 / 2

Active Ingredient

MORPHINE SULFATE

Application Number

201947

Product Number

2

Dosage Form

-

Strength

20MG/5ML

Approval Date

2012-01-05

Regulatory Status

Discontinued

2019
12 Feb
RX Application: 210370

Drug Name

MYCOPHENOLATE MOFETIL

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

2019-02-12

210370 / 1

Active Ingredient

MYCOPHENOLATE MOFETIL

Application Number

210370

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

2019-02-12

Regulatory Status

RX

1998
25 Jun
Discontinued Application: 64142

Drug Name

NYSTATIN

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1998-06-25

64142 / 1

Active Ingredient

NYSTATIN

Application Number

64142

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1998-06-25

Regulatory Status

Discontinued

2011
07 Mar
Discontinued Application: 64142

Drug Name

NYSTATIN

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

2011-03-07

64142 / 2

Active Ingredient

NYSTATIN

Application Number

64142

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

2011-03-07

Regulatory Status

Discontinued

2012
12 Jan
Discontinued Application: 201194

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2012-01-12

201194 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

201194

Product Number

1

Dosage Form

-

Strength

5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2012-01-12

Regulatory Status

Discontinued

2012
30 Jul
Discontinued Application: 202537

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

2012-07-30

202537 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

202537

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

2012-07-30

Regulatory Status

Discontinued

2001
31 Jan
Discontinued Application: 40342

Drug Name

PHENYTOIN

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

2001-01-31

40342 / 1

Active Ingredient

PHENYTOIN

Application Number

40342

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

2001-01-31

Regulatory Status

Discontinued

2005
18 Aug
Discontinued Application: 40342

Drug Name

PHENYTOIN

Product Number

2

Dosage Form

-

Strength

125MG/5ML

Approval Date

2005-08-18

40342 / 2

Active Ingredient

PHENYTOIN

Application Number

40342

Product Number

2

Dosage Form

-

Strength

125MG/5ML

Approval Date

2005-08-18

Regulatory Status

Discontinued

2022
15 Mar
RX Application: 211884

Drug Name

SUCRALFATE

Product Number

1

Dosage Form

-

Strength

1GM/10ML

Approval Date

2022-03-15

211884 / 1

Active Ingredient

SUCRALFATE

Application Number

211884

Product Number

1

Dosage Form

-

Strength

1GM/10ML

Approval Date

2022-03-15

Regulatory Status

RX

2005
07 Oct
RX Application: 76817

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

2005-10-07

76817 / 1

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

76817

Product Number

1

Dosage Form

-

Strength

400MG;80MG

Approval Date

2005-10-07

Regulatory Status

RX

2005
07 Oct
RX Application: 76817

Drug Name

SULFAMETHOXAZOLE AND TRIMETHOPRIM

Product Number

2

Dosage Form

-

Strength

800MG;160MG

Approval Date

2005-10-07

76817 / 2

Active Ingredient

SULFAMETHOXAZOLE; TRIMETHOPRIM

Application Number

76817

Product Number

2

Dosage Form

-

Strength

800MG;160MG

Approval Date

2005-10-07

Regulatory Status

RX

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Drug Status Breakdown
27 total
  • Discontinued
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ACYCLOVIR

Application Number

213951

Product Number

1

Active Ingredient

ACYCLOVIR

Dosage Form

-

Strength

200MG/5ML

FDA Approved Drug Data

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