Vista Pharmaceuticals RX
FDA Approved Drugs

Vista Pharmaceuticals RX

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
  • Total Records 11
  • Latest Approval Date Aug 19, 2022
  • Data Source FDA
  • First Approval Date Nov 30, 1994
All
27
View
Discontinued
16
View
RX
11
View
Company Overview

Company

Vista Pharmaceuticals RX

Country

India

Website

Visit Website

Email

admin.hyd@vistapharmaceuticals.com

Social Profiles

Company Snapshot

Vista Pharmaceuticals RX

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 ( 11 records )
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
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

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
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

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

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

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
11 total
  • RX
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

ARIPIPRAZOLE

Application Number

212870

Product Number

1

Active Ingredient

ARIPIPRAZOLE

Dosage Form

-

Strength

1MG/ML

FDA Approved Drug Data

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