Noven Pharmaceuticals RX
FDA Approved Drugs

Noven Pharmaceuticals 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 15
  • Latest Approval Date Mar 22, 2022
  • Data Source FDA
  • First Approval Date Aug 07, 1998
All
26
View
Unclassified
3
View
Discontinued
8
View
RX
15
View
Company Overview

Company

Noven Pharmaceuticals RX

Country

U.S.A

Website

Visit Website

Email

Social Profiles

Company Snapshot

Noven Pharmaceuticals RX

Noven11960 SW 144th StreetMiami, FL 33186

U.S.A

www.noven.com/ View on Map
FDA Approved Drug Records ( 15 records )
1998
07 Aug
RX Application: 20870

Drug Name

COMBIPATCH

Product Number

1

Dosage Form

-

Strength

0.05MG/24HR;0.14MG/24HR

Approval Date

1998-08-07

20870 / 1

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Application Number

20870

Product Number

1

Dosage Form

-

Strength

0.05MG/24HR;0.14MG/24HR

Approval Date

1998-08-07

Regulatory Status

RX

1998
07 Aug
RX Application: 20870

Drug Name

COMBIPATCH

Product Number

2

Dosage Form

-

Strength

0.05MG/24HR;0.25MG/24HR

Approval Date

1998-08-07

20870 / 2

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Application Number

20870

Product Number

2

Dosage Form

-

Strength

0.05MG/24HR;0.25MG/24HR

Approval Date

1998-08-07

Regulatory Status

RX

2006
06 Apr
RX Application: 21514

Drug Name

DAYTRANA

Product Number

1

Dosage Form

-

Strength

10MG/9HR (1.1MG/HR)

Approval Date

2006-04-06

21514 / 1

Active Ingredient

METHYLPHENIDATE

Application Number

21514

Product Number

1

Dosage Form

-

Strength

10MG/9HR (1.1MG/HR)

Approval Date

2006-04-06

Regulatory Status

RX

2006
06 Apr
RX Application: 21514

Drug Name

DAYTRANA

Product Number

2

Dosage Form

-

Strength

15MG/9HR (1.6MG/HR)

Approval Date

2006-04-06

21514 / 2

Active Ingredient

METHYLPHENIDATE

Application Number

21514

Product Number

2

Dosage Form

-

Strength

15MG/9HR (1.6MG/HR)

Approval Date

2006-04-06

Regulatory Status

RX

2006
06 Apr
RX Application: 21514

Drug Name

DAYTRANA

Product Number

3

Dosage Form

-

Strength

20MG/9HR (2.2MG/HR)

Approval Date

2006-04-06

21514 / 3

Active Ingredient

METHYLPHENIDATE

Application Number

21514

Product Number

3

Dosage Form

-

Strength

20MG/9HR (2.2MG/HR)

Approval Date

2006-04-06

Regulatory Status

RX

2006
06 Apr
RX Application: 21514

Drug Name

DAYTRANA

Product Number

4

Dosage Form

-

Strength

30MG/9HR (3.3MG/HR)

Approval Date

2006-04-06

21514 / 4

Active Ingredient

METHYLPHENIDATE

Application Number

21514

Product Number

4

Dosage Form

-

Strength

30MG/9HR (3.3MG/HR)

Approval Date

2006-04-06

Regulatory Status

RX

2012
29 Oct
RX Application: 203752

Drug Name

MINIVELLE

Product Number

1

Dosage Form

-

Strength

0.0375MG/24HR

Approval Date

2012-10-29

203752 / 1

Active Ingredient

ESTRADIOL

Application Number

203752

Product Number

1

Dosage Form

-

Strength

0.0375MG/24HR

Approval Date

2012-10-29

Regulatory Status

RX

2012
29 Oct
RX Application: 203752

Drug Name

MINIVELLE

Product Number

2

Dosage Form

-

Strength

0.075MG/24HR

Approval Date

2012-10-29

203752 / 2

Active Ingredient

ESTRADIOL

Application Number

203752

Product Number

2

Dosage Form

-

Strength

0.075MG/24HR

Approval Date

2012-10-29

Regulatory Status

RX

2012
29 Oct
RX Application: 203752

Drug Name

MINIVELLE

Product Number

3

Dosage Form

-

Strength

0.05MG/24HR

Approval Date

2012-10-29

203752 / 3

Active Ingredient

ESTRADIOL

Application Number

203752

Product Number

3

Dosage Form

-

Strength

0.05MG/24HR

Approval Date

2012-10-29

Regulatory Status

RX

2012
29 Oct
RX Application: 203752

Drug Name

MINIVELLE

Product Number

4

Dosage Form

-

Strength

0.1MG/24HR

Approval Date

2012-10-29

203752 / 4

Active Ingredient

ESTRADIOL

Application Number

203752

Product Number

4

Dosage Form

-

Strength

0.1MG/24HR

Approval Date

2012-10-29

Regulatory Status

RX

2014
23 Sep
RX Application: 203752

Drug Name

MINIVELLE

Product Number

5

Dosage Form

-

Strength

0.025MG/24HR

Approval Date

2014-09-23

203752 / 5

Active Ingredient

ESTRADIOL

Application Number

203752

Product Number

5

Dosage Form

-

Strength

0.025MG/24HR

Approval Date

2014-09-23

Regulatory Status

RX

2022
22 Mar
RX Application: 215401

Drug Name

XELSTRYM

Product Number

1

Dosage Form

-

Strength

4.5MG/9HR

Approval Date

2022-03-22

215401 / 1

Active Ingredient

DEXTROAMPHETAMINE

Application Number

215401

Product Number

1

Dosage Form

-

Strength

4.5MG/9HR

Approval Date

2022-03-22

Regulatory Status

RX

2022
22 Mar
RX Application: 215401

Drug Name

XELSTRYM

Product Number

2

Dosage Form

-

Strength

9MG/9HR

Approval Date

2022-03-22

215401 / 2

Active Ingredient

DEXTROAMPHETAMINE

Application Number

215401

Product Number

2

Dosage Form

-

Strength

9MG/9HR

Approval Date

2022-03-22

Regulatory Status

RX

2022
22 Mar
RX Application: 215401

Drug Name

XELSTRYM

Product Number

3

Dosage Form

-

Strength

13.5MG/9HR

Approval Date

2022-03-22

215401 / 3

Active Ingredient

DEXTROAMPHETAMINE

Application Number

215401

Product Number

3

Dosage Form

-

Strength

13.5MG/9HR

Approval Date

2022-03-22

Regulatory Status

RX

2022
22 Mar
RX Application: 215401

Drug Name

XELSTRYM

Product Number

4

Dosage Form

-

Strength

18MG/9HR

Approval Date

2022-03-22

215401 / 4

Active Ingredient

DEXTROAMPHETAMINE

Application Number

215401

Product Number

4

Dosage Form

-

Strength

18MG/9HR

Approval Date

2022-03-22

Regulatory Status

RX

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    26 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
15 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

COMBIPATCH

Application Number

20870

Product Number

1

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Dosage Form

-

Strength

0.05MG/24HR;0.14MG/24HR

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit