RK Pharma RX
FDA Approved Drugs

RK Pharma RX

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 16
  • Latest Approval Date Apr 16, 2026
  • Data Source FDA
  • First Approval Date Jan 20, 2016
All
29
View
Unclassified
2
View
Discontinued
11
View
RX
16
View
Company Overview

Company

RK Pharma RX

Country

U.S.A

Website

Visit Website

Email

support@rkpharmainc.com

Social Profiles

Company Snapshot

RK Pharma RX

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 ( 16 records )
2016
20 Jan
RX Application: 202337

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE

Approval Date

2016-01-20

202337 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

202337

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE

Approval Date

2016-01-20

Regulatory Status

RX

2016
20 Jan
RX Application: 202337

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 6MG BASE

Approval Date

2016-01-20

202337 / 2

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

202337

Product Number

2

Dosage Form

-

Strength

EQ 6MG BASE

Approval Date

2016-01-20

Regulatory Status

RX

2017
13 Oct
RX Application: 202670

Drug Name

MITOMYCIN

Product Number

1

Dosage Form

-

Strength

5MG/VIAL

Approval Date

2017-10-13

202670 / 1

Active Ingredient

MITOMYCIN

Application Number

202670

Product Number

1

Dosage Form

-

Strength

5MG/VIAL

Approval Date

2017-10-13

Regulatory Status

RX

2017
13 Oct
RX Application: 202670

Drug Name

MITOMYCIN

Product Number

2

Dosage Form

-

Strength

20MG/VIAL

Approval Date

2017-10-13

202670 / 2

Active Ingredient

MITOMYCIN

Application Number

202670

Product Number

2

Dosage Form

-

Strength

20MG/VIAL

Approval Date

2017-10-13

Regulatory Status

RX

2017
13 Oct
RX Application: 203386

Drug Name

MITOMYCIN

Product Number

1

Dosage Form

-

Strength

40MG/VIAL

Approval Date

2017-10-13

203386 / 1

Active Ingredient

MITOMYCIN

Application Number

203386

Product Number

1

Dosage Form

-

Strength

40MG/VIAL

Approval Date

2017-10-13

Regulatory Status

RX

2019
13 Sep
RX Application: 212856

Drug Name

NADOLOL

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2019-09-13

212856 / 1

Active Ingredient

NADOLOL

Application Number

212856

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2019-09-13

Regulatory Status

RX

2019
13 Sep
RX Application: 212856

Drug Name

NADOLOL

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2019-09-13

212856 / 2

Active Ingredient

NADOLOL

Application Number

212856

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2019-09-13

Regulatory Status

RX

2019
13 Sep
RX Application: 212856

Drug Name

NADOLOL

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

2019-09-13

212856 / 3

Active Ingredient

NADOLOL

Application Number

212856

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

2019-09-13

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

2026-04-16

214055 / 1

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

1

Dosage Form

-

Strength

0.2MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

2

Dosage Form

-

Strength

0.4MG

Approval Date

2026-04-16

214055 / 2

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

2

Dosage Form

-

Strength

0.4MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

3

Dosage Form

-

Strength

0.6MG

Approval Date

2026-04-16

214055 / 3

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

3

Dosage Form

-

Strength

0.6MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

4

Dosage Form

-

Strength

0.8MG

Approval Date

2026-04-16

214055 / 4

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

4

Dosage Form

-

Strength

0.8MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

5

Dosage Form

-

Strength

1MG

Approval Date

2026-04-16

214055 / 5

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

5

Dosage Form

-

Strength

1MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

6

Dosage Form

-

Strength

1.2MG

Approval Date

2026-04-16

214055 / 6

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

6

Dosage Form

-

Strength

1.2MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

7

Dosage Form

-

Strength

1.4MG

Approval Date

2026-04-16

214055 / 7

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

7

Dosage Form

-

Strength

1.4MG

Approval Date

2026-04-16

Regulatory Status

RX

2026
16 Apr
RX Application: 214055

Drug Name

SELEXIPAG

Product Number

8

Dosage Form

-

Strength

1.6MG

Approval Date

2026-04-16

214055 / 8

Active Ingredient

SELEXIPAG

Application Number

214055

Product Number

8

Dosage Form

-

Strength

1.6MG

Approval Date

2026-04-16

Regulatory Status

RX

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Drug Status Breakdown
16 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

DOXEPIN HYDROCHLORIDE

Application Number

202337

Product Number

1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Dosage Form

-

Strength

EQ 3MG BASE

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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