Esjay Pharma
FDA Approved Drugs

Esjay Pharma

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 Jul 28, 2026
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Esjay Pharma

Country

India

Website

Visit Website

Email

info@esjaypharma.com

Social Profiles

Company Snapshot

Esjay Pharma

Plot No G28 & 29, 12th Main Road, Tamil Nadu

India

www.esjaypharma.com/ info@esjaypharma.com View on Map
FDA Approved Drug Records ( 11 records )
1982
01 Jan
RX Application: 3444

Drug Name

DRISDOL

Product Number

1

Dosage Form

-

Strength

50,000 IU

Approval Date

1982-01-01

3444 / 1

Active Ingredient

ERGOCALCIFEROL

Application Number

3444

Product Number

1

Dosage Form

-

Strength

50,000 IU

Approval Date

1982-01-01

Regulatory Status

RX

1982
27 Jul
RX Application: 18415

Drug Name

FUROSEMIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-07-27

18415 / 1

Active Ingredient

FUROSEMIDE

Application Number

18415

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-07-27

Regulatory Status

RX

1982
27 Jul
RX Application: 18415

Drug Name

FUROSEMIDE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

1982-07-27

18415 / 2

Active Ingredient

FUROSEMIDE

Application Number

18415

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

1982-07-27

Regulatory Status

RX

1984
26 Nov
RX Application: 18415

Drug Name

FUROSEMIDE

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

1984-11-26

18415 / 3

Active Ingredient

FUROSEMIDE

Application Number

18415

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

1984-11-26

Regulatory Status

RX

2026
28 Jul
RX Application: 220579

Drug Name

GLYCEROL PHENYLBUTYRATE

Product Number

1

Dosage Form

-

Strength

1.1GM/ML

Approval Date

2026-07-28

220579 / 1

Active Ingredient

GLYCEROL PHENYLBUTYRATE

Application Number

220579

Product Number

1

Dosage Form

-

Strength

1.1GM/ML

Approval Date

2026-07-28

Regulatory Status

RX

1982
01 Jan
RX Application: 17681

Drug Name

HIPREX

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

1982-01-01

17681 / 1

Active Ingredient

METHENAMINE HIPPURATE

Application Number

17681

Product Number

1

Dosage Form

-

Strength

1GM

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 17962

Drug Name

PARLODEL

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

1982-01-01

17962 / 1

Active Ingredient

BROMOCRIPTINE MESYLATE

Application Number

17962

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Mar
RX Application: 17962

Drug Name

PARLODEL

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1982-03-01

17962 / 2

Active Ingredient

BROMOCRIPTINE MESYLATE

Application Number

17962

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

1982-03-01

Regulatory Status

RX

1982
01 Jan
RX Application: 18044

Drug Name

ROCALTROL

Product Number

1

Dosage Form

-

Strength

0.25MCG

Approval Date

1982-01-01

18044 / 1

Active Ingredient

CALCITRIOL

Application Number

18044

Product Number

1

Dosage Form

-

Strength

0.25MCG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 18044

Drug Name

ROCALTROL

Product Number

2

Dosage Form

-

Strength

0.5MCG

Approval Date

1982-01-01

18044 / 2

Active Ingredient

CALCITRIOL

Application Number

18044

Product Number

2

Dosage Form

-

Strength

0.5MCG

Approval Date

1982-01-01

Regulatory Status

RX

1998
20 Nov
RX Application: 21068

Drug Name

ROCALTROL

Product Number

1

Dosage Form

-

Strength

1MCG/ML

Approval Date

1998-11-20

21068 / 1

Active Ingredient

CALCITRIOL

Application Number

21068

Product Number

1

Dosage Form

-

Strength

1MCG/ML

Approval Date

1998-11-20

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

DRISDOL

Application Number

3444

Product Number

1

Active Ingredient

ERGOCALCIFEROL

Dosage Form

-

Strength

50,000 IU

FDA Approved Drug Data

Approved drug product information

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