Dey
FDA Approved Drugs

Dey

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 16
  • Latest Approval Date Nov 22, 1988
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Dey

Country

India

Website

Visit Website

Email

mkt2@deysmedical.com

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Company Snapshot

Dey

62, Bondel Road ,Kolkata - 700 019

India

www.deysmedical.com/ mkt2@deysmedical.com View on Map
FDA Approved Drug Records ( 16 records )
1982
01 Jan
Discontinued Application: 86763

Drug Name

ISOETHARINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

86763 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

86763

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87389

Drug Name

ISOETHARINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

87389 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

87389

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87390

Drug Name

ISOETHARINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.17%

Approval Date

1982-01-01

87390 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

87390

Product Number

1

Dosage Form

-

Strength

0.17%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
03 Dec
Discontinued Application: 88187

Drug Name

ISOETHARINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.08%

Approval Date

1982-12-03

88187 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

88187

Product Number

1

Dosage Form

-

Strength

0.08%

Approval Date

1982-12-03

Regulatory Status

Discontinued

1982
03 Dec
Discontinued Application: 88188

Drug Name

ISOETHARINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1982-12-03

88188 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

88188

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1982-12-03

Regulatory Status

Discontinued

1986
15 Sep
Discontinued Application: 89252

Drug Name

ISOETHARINE HYDROCHLORIDE S/F

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1986-09-15

89252 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

89252

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1986-09-15

Regulatory Status

Discontinued

1988
22 Nov
Discontinued Application: 89817

Drug Name

ISOETHARINE HYDROCHLORIDE S/F

Product Number

1

Dosage Form

-

Strength

0.08%

Approval Date

1988-11-22

89817 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

89817

Product Number

1

Dosage Form

-

Strength

0.08%

Approval Date

1988-11-22

Regulatory Status

Discontinued

1988
22 Nov
Discontinued Application: 89818

Drug Name

ISOETHARINE HYDROCHLORIDE S/F

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1988-11-22

89818 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

89818

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1988-11-22

Regulatory Status

Discontinued

1988
22 Nov
Discontinued Application: 89819

Drug Name

ISOETHARINE HYDROCHLORIDE S/F

Product Number

1

Dosage Form

-

Strength

0.17%

Approval Date

1988-11-22

89819 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

89819

Product Number

1

Dosage Form

-

Strength

0.17%

Approval Date

1988-11-22

Regulatory Status

Discontinued

1988
22 Nov
Discontinued Application: 89820

Drug Name

ISOETHARINE HYDROCHLORIDE S/F

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1988-11-22

89820 / 1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Application Number

89820

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1988-11-22

Regulatory Status

Discontinued

1982
04 Jan
Discontinued Application: 86764

Drug Name

ISOPROTERENOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-04

86764 / 1

Active Ingredient

ISOPROTERENOL HYDROCHLORIDE

Application Number

86764

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-04

Regulatory Status

Discontinued

1987
17 Aug
Discontinued Application: 70805

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

1987-08-17

70805 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

70805

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

1987-08-17

Regulatory Status

Discontinued

1988
05 Aug
Discontinued Application: 71805

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1988-08-05

71805 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

71805

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1988-08-05

Regulatory Status

Discontinued

1988
05 Aug
Discontinued Application: 71806

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

0.33%

Approval Date

1988-08-05

71806 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

71806

Product Number

1

Dosage Form

-

Strength

0.33%

Approval Date

1988-08-05

Regulatory Status

Discontinued

1986
14 Oct
Discontinued Application: 70575

Drug Name

MUCOSIL-10

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1986-10-14

70575 / 1

Active Ingredient

ACETYLCYSTEINE

Application Number

70575

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1986-10-14

Regulatory Status

Discontinued

1986
14 Oct
Discontinued Application: 70576

Drug Name

MUCOSIL-20

Product Number

1

Dosage Form

-

Strength

20%

Approval Date

1986-10-14

70576 / 1

Active Ingredient

ACETYLCYSTEINE

Application Number

70576

Product Number

1

Dosage Form

-

Strength

20%

Approval Date

1986-10-14

Regulatory Status

Discontinued

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Drug Status Breakdown
16 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

ISOETHARINE HYDROCHLORIDE

Application Number

86763

Product Number

1

Active Ingredient

ISOETHARINE HYDROCHLORIDE

Dosage Form

-

Strength

1%

FDA Approved Drug Data

Approved drug product information

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