The Ritedose Corporation
FDA Approved Drugs

The Ritedose Corporation

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 11
  • Latest Approval Date Mar 12, 2025
  • Data Source FDA
  • First Approval Date Jan 26, 2001
Company Overview

Company

The Ritedose Corporation

Country

U.S.A

Website

Visit Website

Email

paynem@ritedose.com

Social Profiles

Company Snapshot

The Ritedose Corporation

Carolina Research Park, 1 Technology Circle, Columbia, SC 29203, USA

U.S.A

ritedose.com/ paynem@ritedose.com View on Map
FDA Approved Drug Records ( 11 records )
2008
16 Dec
RX Application: 77839

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

2008-12-16

77839 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

77839

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

2008-12-16

Regulatory Status

RX

2021
28 Dec
RX Application: 214531

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2021-12-28

214531 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

214531

Product Number

1

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2021-12-28

Regulatory Status

RX

2021
28 Dec
RX Application: 214531

Drug Name

ALBUTEROL SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2021-12-28

214531 / 2

Active Ingredient

ALBUTEROL SULFATE

Application Number

214531

Product Number

2

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2021-12-28

Regulatory Status

RX

2025
12 Mar
RX Application: 218386

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2025-03-12

218386 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

218386

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2025-03-12

Regulatory Status

RX

2012
01 Oct
RX Application: 202496

Drug Name

ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2012-10-01

202496 / 1

Active Ingredient

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Application Number

202496

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2012-10-01

Regulatory Status

RX

2022
02 Mar
RX Application: 214736

Drug Name

ARFORMOTEROL TARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 0.015MG BASE/2ML

Approval Date

2022-03-02

214736 / 1

Active Ingredient

ARFORMOTEROL TARTRATE

Application Number

214736

Product Number

1

Dosage Form

-

Strength

EQ 0.015MG BASE/2ML

Approval Date

2022-03-02

Regulatory Status

RX

2022
25 Nov
RX Application: 216486

Drug Name

FORMOTEROL FUMARATE

Product Number

1

Dosage Form

-

Strength

0.02MG/2ML

Approval Date

2022-11-25

216486 / 1

Active Ingredient

FORMOTEROL FUMARATE

Application Number

216486

Product Number

1

Dosage Form

-

Strength

0.02MG/2ML

Approval Date

2022-11-25

Regulatory Status

RX

2001
26 Jan
RX Application: 75693

Drug Name

IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2001-01-26

75693 / 1

Active Ingredient

IPRATROPIUM BROMIDE

Application Number

75693

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2001-01-26

Regulatory Status

RX

2016
22 Mar
RX Application: 203653

Drug Name

LEVALBUTEROL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.0103% BASE

Approval Date

2016-03-22

203653 / 1

Active Ingredient

LEVALBUTEROL HYDROCHLORIDE

Application Number

203653

Product Number

1

Dosage Form

-

Strength

EQ 0.0103% BASE

Approval Date

2016-03-22

Regulatory Status

RX

2016
22 Mar
RX Application: 203653

Drug Name

LEVALBUTEROL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2016-03-22

203653 / 2

Active Ingredient

LEVALBUTEROL HYDROCHLORIDE

Application Number

203653

Product Number

2

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2016-03-22

Regulatory Status

RX

2016
22 Mar
RX Application: 203653

Drug Name

LEVALBUTEROL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2016-03-22

203653 / 3

Active Ingredient

LEVALBUTEROL HYDROCHLORIDE

Application Number

203653

Product Number

3

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2016-03-22

Regulatory Status

RX

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Drug Status Breakdown
11 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

ALBUTEROL SULFATE

Application Number

77839

Product Number

1

Active Ingredient

ALBUTEROL SULFATE

Dosage Form

-

Strength

EQ 0.083% BASE

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

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