Xiromed Discontinued
FDA Approved Drugs

Xiromed Discontinued

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 19
  • Latest Approval Date Aug 20, 2021
  • Data Source FDA
  • First Approval Date Aug 05, 2013
All
99
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Discontinued
19
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OTC
2
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RX
78
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Company

Xiromed Discontinued

Country

U.S.A

Website

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Xiromed Discontinued

180 Park Ave ,Suite 101 Florham Park, NJ 07932

U.S.A

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FDA Approved Drug Records ( 19 records )
2021
20 Aug
Discontinued Application: 215046

Drug Name

CYANOCOBALAMIN

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2021-08-20

215046 / 1

Active Ingredient

CYANOCOBALAMIN

Application Number

215046

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2021-08-20

Regulatory Status

Discontinued

2019
22 Oct
Discontinued Application: 209571

Drug Name

DARIFENACIN HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2019-10-22

209571 / 1

Active Ingredient

DARIFENACIN HYDROBROMIDE

Application Number

209571

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2019-10-22

Regulatory Status

Discontinued

2019
22 Oct
Discontinued Application: 209571

Drug Name

DARIFENACIN HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 7.5MG BASE

Approval Date

2019-10-22

209571 / 2

Active Ingredient

DARIFENACIN HYDROBROMIDE

Application Number

209571

Product Number

2

Dosage Form

-

Strength

EQ 7.5MG BASE

Approval Date

2019-10-22

Regulatory Status

Discontinued

2015
20 May
Discontinued Application: 202085

Drug Name

DESOGESTREL AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.15MG;0.03MG

Approval Date

2015-05-20

202085 / 1

Active Ingredient

DESOGESTREL; ETHINYL ESTRADIOL

Application Number

202085

Product Number

1

Dosage Form

-

Strength

0.15MG;0.03MG

Approval Date

2015-05-20

Regulatory Status

Discontinued

2015
04 Dec
Discontinued Application: 202507

Drug Name

ELIFEMME

Product Number

1

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2015-12-04

202507 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

202507

Product Number

1

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2015-12-04

Regulatory Status

Discontinued

2021
04 Mar
Discontinued Application: 212227

Drug Name

GLYCOPYRROLATE

Product Number

1

Dosage Form

-

Strength

0.2MG/ML

Approval Date

2021-03-04

212227 / 1

Active Ingredient

GLYCOPYRROLATE

Application Number

212227

Product Number

1

Dosage Form

-

Strength

0.2MG/ML

Approval Date

2021-03-04

Regulatory Status

Discontinued

2016
02 Sep
Discontinued Application: 202740

Drug Name

LEVONORGESTREL

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

2016-09-02

202740 / 1

Active Ingredient

LEVONORGESTREL

Application Number

202740

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

2016-09-02

Regulatory Status

Discontinued

2014
08 Dec
Discontinued Application: 202247

Drug Name

LEVONORGESTREL AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2014-12-08

202247 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

202247

Product Number

1

Dosage Form

-

Strength

0.02MG;0.1MG

Approval Date

2014-12-08

Regulatory Status

Discontinued

2018
23 Mar
Discontinued Application: 202970

Drug Name

LEVONORGESTREL AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2018-03-23

202970 / 1

Active Ingredient

ETHINYL ESTRADIOL; LEVONORGESTREL

Application Number

202970

Product Number

1

Dosage Form

-

Strength

0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG

Approval Date

2018-03-23

Regulatory Status

Discontinued

2016
27 Dec
Discontinued Application: 207259

Drug Name

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.005MG;1MG

Approval Date

2016-12-27

207259 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

207259

Product Number

1

Dosage Form

-

Strength

0.005MG;1MG

Approval Date

2016-12-27

Regulatory Status

Discontinued

2017
02 Feb
Discontinued Application: 207260

Drug Name

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.0025MG;0.5MG

Approval Date

2017-02-02

207260 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

207260

Product Number

1

Dosage Form

-

Strength

0.0025MG;0.5MG

Approval Date

2017-02-02

Regulatory Status

Discontinued

2016
31 May
Discontinued Application: 205049

Drug Name

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL AND FERROUS FUMARATE

Product Number

1

Dosage Form

-

Strength

0.01MG,0.01MG;1MG,N/A

Approval Date

2016-05-31

205049 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

205049

Product Number

1

Dosage Form

-

Strength

0.01MG,0.01MG;1MG,N/A

Approval Date

2016-05-31

Regulatory Status

Discontinued

2014
30 Oct
Discontinued Application: 202742

Drug Name

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2014-10-30

202742 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

202742

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2014-10-30

Regulatory Status

Discontinued

2017
12 Sep
Discontinued Application: 206120

Drug Name

NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2017-09-12

206120 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

206120

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2017-09-12

Regulatory Status

Discontinued

2015
11 May
Discontinued Application: 200897

Drug Name

NORETHINDRONE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2015-05-11

200897 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

200897

Product Number

1

Dosage Form

-

Strength

0.035MG;0.4MG

Approval Date

2015-05-11

Regulatory Status

Discontinued

2013
05 Aug
Discontinued Application: 203006

Drug Name

NORETHINDRONE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG

Approval Date

2013-08-05

203006 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE

Application Number

203006

Product Number

1

Dosage Form

-

Strength

0.05MG;1MG

Approval Date

2013-08-05

Regulatory Status

Discontinued

2016
27 Jan
Discontinued Application: 201897

Drug Name

NORGESTIMATE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG

Approval Date

2016-01-27

201897 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORGESTIMATE

Application Number

201897

Product Number

1

Dosage Form

-

Strength

0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG

Approval Date

2016-01-27

Regulatory Status

Discontinued

2015
09 Sep
Discontinued Application: 202132

Drug Name

NORGESTIMATE AND ETHINYL ESTRADIOL

Product Number

1

Dosage Form

-

Strength

0.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG

Approval Date

2015-09-09

202132 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORGESTIMATE

Application Number

202132

Product Number

1

Dosage Form

-

Strength

0.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG

Approval Date

2015-09-09

Regulatory Status

Discontinued

2020
29 Oct
Discontinued Application: 211277

Drug Name

SODIUM NITROPRUSSIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

2020-10-29

211277 / 1

Active Ingredient

SODIUM NITROPRUSSIDE

Application Number

211277

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

2020-10-29

Regulatory Status

Discontinued

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Drug Status Breakdown
19 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

CYANOCOBALAMIN

Application Number

215046

Product Number

1

Active Ingredient

CYANOCOBALAMIN

Dosage Form

-

Strength

1MG/ML

FDA Approved Drug Data

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