RK Pharma Discontinued
FDA Approved Drugs

RK Pharma 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 11
  • Latest Approval Date Aug 16, 2021
  • Data Source FDA
  • First Approval Date Jan 08, 2014
All
29
View
Unclassified
2
View
Discontinued
11
View
RX
16
View
Company Overview

Company

RK Pharma Discontinued

Country

U.S.A

Website

Visit Website

Email

support@rkpharmainc.com

Social Profiles

Company Snapshot

RK Pharma Discontinued

401 North Middletown Road, Building 215/215A Pearl River, NY 10965

U.S.A

rkpharmainc.com/ support@rkpharmainc.com View on Map
FDA Approved Drug Records ( 11 records )
2021
16 Aug
Discontinued Application: 214328

Drug Name

CARBAMAZEPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2021-08-16

214328 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

214328

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2021-08-16

Regulatory Status

Discontinued

2014
18 Jun
Discontinued Application: 202493

Drug Name

CHLOROTHIAZIDE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2014-06-18

202493 / 1

Active Ingredient

CHLOROTHIAZIDE SODIUM

Application Number

202493

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2014-06-18

Regulatory Status

Discontinued

2020
22 Jun
Discontinued Application: 213221

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2020-06-22

213221 / 1

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

213221

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2020-06-22

Regulatory Status

Discontinued

2020
22 Jun
Discontinued Application: 213221

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2020-06-22

213221 / 2

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

213221

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2020-06-22

Regulatory Status

Discontinued

2020
22 Jun
Discontinued Application: 213221

Drug Name

CLOMIPRAMINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2020-06-22

213221 / 3

Active Ingredient

CLOMIPRAMINE HYDROCHLORIDE

Application Number

213221

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2020-06-22

Regulatory Status

Discontinued

2014
08 Jan
Discontinued Application: 91248

Drug Name

MYCOPHENOLATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 360MG BASE

Approval Date

2014-01-08

91248 / 1

Active Ingredient

MYCOPHENOLATE SODIUM

Application Number

91248

Product Number

1

Dosage Form

-

Strength

EQ 360MG BASE

Approval Date

2014-01-08

Regulatory Status

Discontinued

2014
08 Jan
Discontinued Application: 91248

Drug Name

MYCOPHENOLATE SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 180MG BASE

Approval Date

2014-01-08

91248 / 2

Active Ingredient

MYCOPHENOLATE SODIUM

Application Number

91248

Product Number

2

Dosage Form

-

Strength

EQ 180MG BASE

Approval Date

2014-01-08

Regulatory Status

Discontinued

2015
24 Sep
Discontinued Application: 203802

Drug Name

PALIPERIDONE

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

2015-09-24

203802 / 1

Active Ingredient

PALIPERIDONE

Application Number

203802

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

2015-09-24

Regulatory Status

Discontinued

2015
24 Sep
Discontinued Application: 203802

Drug Name

PALIPERIDONE

Product Number

2

Dosage Form

-

Strength

3MG

Approval Date

2015-09-24

203802 / 2

Active Ingredient

PALIPERIDONE

Application Number

203802

Product Number

2

Dosage Form

-

Strength

3MG

Approval Date

2015-09-24

Regulatory Status

Discontinued

2015
24 Sep
Discontinued Application: 203802

Drug Name

PALIPERIDONE

Product Number

3

Dosage Form

-

Strength

6MG

Approval Date

2015-09-24

203802 / 3

Active Ingredient

PALIPERIDONE

Application Number

203802

Product Number

3

Dosage Form

-

Strength

6MG

Approval Date

2015-09-24

Regulatory Status

Discontinued

2015
24 Sep
Discontinued Application: 203802

Drug Name

PALIPERIDONE

Product Number

4

Dosage Form

-

Strength

9MG

Approval Date

2015-09-24

203802 / 4

Active Ingredient

PALIPERIDONE

Application Number

203802

Product Number

4

Dosage Form

-

Strength

9MG

Approval Date

2015-09-24

Regulatory Status

Discontinued

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Drug Status Breakdown
11 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

CARBAMAZEPINE

Application Number

214328

Product Number

1

Active Ingredient

CARBAMAZEPINE

Dosage Form

-

Strength

200MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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