Pharmaderm
FDA Approved Drugs

Pharmaderm

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 26
Latest Approval Date Feb 09, 1987
Data Source FDA
First Approval Date Jan 01, 1982

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Company

Pharmaderm

Country

U.S.A

Website

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info@pharmaderm.co

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Company Snapshot

Pharmaderm

Melville, New York

U.S.A

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FDA Approved Drug Records ( 26 records )

1982

01 Jan

Discontinued Application: 62158

Drug Name

BACITRACIN

Product Number

Dosage Form

Strength

500 UNITS/GM

Approval Date

1982-01-01

62158 / 1 View Details

Active Ingredient

BACITRACIN

Application Number

62158

Product Number

Dosage Form

Strength

500 UNITS/GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62167

Drug Name

BACITRACIN-NEOMYCIN-POLYMYXIN

Product Number

Dosage Form

Strength

400 UNITS/GM;EQ 3.5MG BASE/GM;5,000 UNITS/GM

Approval Date

1982-01-01

62167 / 1 View Details

Active Ingredient

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62167

Product Number

Dosage Form

Strength

400 UNITS/GM;EQ 3.5MG BASE/GM;5,000 UNITS/GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984

26 Jun

Discontinued Application: 19136

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

Dosage Form

Strength

EQ 0.05% BASE

Approval Date

1984-06-26

19136 / 1 View Details

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

19136

Product Number

Dosage Form

Strength

EQ 0.05% BASE

Approval Date

1984-06-26

Regulatory Status

Discontinued

1984

04 Sep

Discontinued Application: 19140

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

Dosage Form

Strength

EQ 0.05% BASE

Approval Date

1984-09-04

19140 / 1 View Details

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

19140

Product Number

Dosage Form

Strength

EQ 0.05% BASE

Approval Date

1984-09-04

Regulatory Status

Discontinued

1983

31 Aug

Discontinued Application: 18860

Drug Name

BETAMETHASONE VALERATE

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1983-08-31

18860 / 2 View Details

Active Ingredient

BETAMETHASONE VALERATE

Application Number

18860

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1983-08-31

Regulatory Status

Discontinued

1983

31 Aug

Discontinued Application: 18864

Drug Name

BETAMETHASONE VALERATE

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1983-08-31

18864 / 1 View Details

Active Ingredient

BETAMETHASONE VALERATE

Application Number

18864

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1983-08-31

Regulatory Status

Discontinued

1983

31 Aug

Discontinued Application: 18870

Drug Name

BETAMETHASONE VALERATE

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1983-08-31

18870 / 1 View Details

Active Ingredient

BETAMETHASONE VALERATE

Application Number

18870

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1983-08-31

Regulatory Status

Discontinued

1983

26 Sep

Discontinued Application: 62446

Drug Name

ERYTHROMYCIN

Product Number

Dosage Form

Strength

5MG/GM

Approval Date

1983-09-26

62446 / 1 View Details

Active Ingredient

ERYTHROMYCIN

Application Number

62446

Product Number

Dosage Form

Strength

5MG/GM

Approval Date

1983-09-26

Regulatory Status

Discontinued

1982

16 Dec

Discontinued Application: 88046

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.025%

Approval Date

1982-12-16

88046 / 1 View Details

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88046

Product Number

Dosage Form

Strength

0.025%

Approval Date

1982-12-16

Regulatory Status

Discontinued

1984

05 Jul

Discontinued Application: 62530

Drug Name

GENTAMICIN SULFATE

Product Number

Dosage Form

Strength

EQ 1MG BASE/GM

Approval Date

1984-07-05

62530 / 1 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62530

Product Number

Dosage Form

Strength

EQ 1MG BASE/GM

Approval Date

1984-07-05

Regulatory Status

Discontinued

1984

10 Oct

Discontinued Application: 62534

Drug Name

GENTAMICIN SULFATE

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1984-10-10

62534 / 1 View Details

Active Ingredient

GENTAMICIN SULFATE

Application Number

62534

Product Number

Dosage Form

Strength

EQ 0.1% BASE

Approval Date

1984-10-10

Regulatory Status

Discontinued

1987

09 Feb

Discontinued Application: 88842

Drug Name

HYDROCORTISONE

Product Number

Dosage Form

Strength

Approval Date

1987-02-09

88842 / 1 View Details

Active Ingredient

HYDROCORTISONE

Application Number

88842

Product Number

Dosage Form

Strength

Approval Date

1987-02-09

Regulatory Status

Discontinued

1986

27 Feb

Discontinued Application: 88845

Drug Name

HYDROCORTISONE

Product Number

Dosage Form

Strength

Approval Date

1986-02-27

88845 / 1 View Details

Active Ingredient

HYDROCORTISONE

Application Number

88845

Product Number

Dosage Form

Strength

Approval Date

1986-02-27

Regulatory Status

Discontinued

1986

16 Dec

Discontinued Application: 89413

Drug Name

HYDROCORTISONE

Product Number

Dosage Form

Strength

2.5%

Approval Date

1986-12-16

89413 / 1 View Details

Active Ingredient

HYDROCORTISONE

Application Number

89413

Product Number

Dosage Form

Strength

2.5%

Approval Date

1986-12-16

Regulatory Status

Discontinued

1986

21 Jul

Discontinued Application: 62595

Drug Name

NEOMYCIN SULFATE-TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

EQ 3.5MG BASE/GM;0.1%

Approval Date

1986-07-21

62595 / 1 View Details

Active Ingredient

NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE

Application Number

62595

Product Number

Dosage Form

Strength

EQ 3.5MG BASE/GM;0.1%

Approval Date

1986-07-21

Regulatory Status

Discontinued

1986

23 May

Discontinued Application: 62607

Drug Name

NEOMYCIN SULFATE-TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

EQ 3.5MG BASE/GM;0.1%

Approval Date

1986-05-23

62607 / 1 View Details

Active Ingredient

NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE

Application Number

62607

Product Number

Dosage Form

Strength

EQ 3.5MG BASE/GM;0.1%

Approval Date

1986-05-23

Regulatory Status

Discontinued

1983

09 Nov

Discontinued Application: 62460

Drug Name

NYSTATIN

Product Number

Dosage Form

Strength

100,000 UNITS

Approval Date

1983-11-09

62460 / 1 View Details

Active Ingredient

NYSTATIN

Application Number

62460

Product Number

Dosage Form

Strength

100,000 UNITS

Approval Date

1983-11-09

Regulatory Status

Discontinued

1984

06 Jul

Discontinued Application: 62518

Drug Name

NYSTATIN

Product Number

Dosage Form

Strength

100,000 UNITS/ML

Approval Date

1984-07-06

62518 / 1 View Details

Active Ingredient

NYSTATIN

Application Number

62518

Product Number

Dosage Form

Strength

100,000 UNITS/ML

Approval Date

1984-07-06

Regulatory Status

Discontinued

1985

08 Oct

Discontinued Application: 62596

Drug Name

NYSTATIN TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-10-08

62596 / 1 View Details

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62596

Product Number

Dosage Form

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-10-08

Regulatory Status

Discontinued

1985

09 Oct

Discontinued Application: 62603

Drug Name

NYSTATIN-TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-10-09

62603 / 1 View Details

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62603

Product Number

Dosage Form

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-10-09

Regulatory Status

Discontinued

1983

07 Jul

Discontinued Application: 87990

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.025%

Approval Date

1983-07-07

87990 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87990

Product Number

Dosage Form

Strength

0.025%

Approval Date

1983-07-07

Regulatory Status

Discontinued

1983

07 Jul

Discontinued Application: 87991

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.1%

Approval Date

1983-07-07

87991 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87991

Product Number

Dosage Form

Strength

0.1%

Approval Date

1983-07-07

Regulatory Status

Discontinued

1983

07 Jul

Discontinued Application: 87992

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.5%

Approval Date

1983-07-07

87992 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87992

Product Number

Dosage Form

Strength

0.5%

Approval Date

1983-07-07

Regulatory Status

Discontinued

1984

02 Aug

Discontinued Application: 88690

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.1%

Approval Date

1984-08-02

88690 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88690

Product Number

Dosage Form

Strength

0.1%

Approval Date

1984-08-02

Regulatory Status

Discontinued

1984

02 Aug

Discontinued Application: 88692

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.025%

Approval Date

1984-08-02

88692 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88692

Product Number

Dosage Form

Strength

0.025%

Approval Date

1984-08-02

Regulatory Status

Discontinued

1985

03 Jan

Discontinued Application: 88462

Drug Name

TRIPLE SULFA

Product Number

Dosage Form

Strength

184MG;143.75MG;172.5MG

Approval Date

1985-01-03

88462 / 1 View Details

Active Ingredient

TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)

Application Number

88462

Product Number

Dosage Form

Strength

184MG;143.75MG;172.5MG

Approval Date

1985-01-03

Regulatory Status

Discontinued

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Drug Status Breakdown

26 total

Discontinued

Official Source

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Drug Name

BACITRACIN

Application Number

62158

Product Number

Active Ingredient

BACITRACIN

Dosage Form

Strength

500 UNITS/GM

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