Tolmar RX
FDA Approved Drugs

Tolmar 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 8
  • Latest Approval Date May 01, 2020
  • Data Source FDA
  • First Approval Date Jan 23, 2002
All
15
View
Unclassified
5
View
Discontinued
2
View
RX
8
View
Company Overview

Company

Tolmar RX

Country

U.S.A

Social Profiles

Company Snapshot

Tolmar RX

701 Centre Ave, Fort Collins, CO 80526

U.S.A

www.tolmar.com/ info@tolmar.com View on Map
FDA Approved Drug Records ( 8 records )
2002
23 Jan
RX Application: 21343

Drug Name

ELIGARD KIT

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2002-01-23

21343 / 1

Active Ingredient

LEUPROLIDE ACETATE

Application Number

21343

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2002-01-23

Regulatory Status

RX

2002
24 Jul
RX Application: 21379

Drug Name

ELIGARD KIT

Product Number

1

Dosage Form

-

Strength

22.5MG

Approval Date

2002-07-24

21379 / 1

Active Ingredient

LEUPROLIDE ACETATE

Application Number

21379

Product Number

1

Dosage Form

-

Strength

22.5MG

Approval Date

2002-07-24

Regulatory Status

RX

2003
13 Feb
RX Application: 21488

Drug Name

ELIGARD KIT

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2003-02-13

21488 / 1

Active Ingredient

LEUPROLIDE ACETATE

Application Number

21488

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2003-02-13

Regulatory Status

RX

2004
14 Dec
RX Application: 21731

Drug Name

ELIGARD KIT

Product Number

1

Dosage Form

-

Strength

45MG

Approval Date

2004-12-14

21731 / 1

Active Ingredient

LEUPROLIDE ACETATE

Application Number

21731

Product Number

1

Dosage Form

-

Strength

45MG

Approval Date

2004-12-14

Regulatory Status

RX

2020
01 May
RX Application: 213150

Drug Name

FENSOLVI KIT

Product Number

1

Dosage Form

-

Strength

45MG

Approval Date

2020-05-01

213150 / 1

Active Ingredient

LEUPROLIDE ACETATE

Application Number

213150

Product Number

1

Dosage Form

-

Strength

45MG

Approval Date

2020-05-01

Regulatory Status

RX

2019
27 Mar
RX Application: 206089

Drug Name

JATENZO

Product Number

1

Dosage Form

-

Strength

158MG

Approval Date

2019-03-27

206089 / 1

Active Ingredient

TESTOSTERONE UNDECANOATE

Application Number

206089

Product Number

1

Dosage Form

-

Strength

158MG

Approval Date

2019-03-27

Regulatory Status

RX

2019
27 Mar
RX Application: 206089

Drug Name

JATENZO

Product Number

2

Dosage Form

-

Strength

198MG

Approval Date

2019-03-27

206089 / 2

Active Ingredient

TESTOSTERONE UNDECANOATE

Application Number

206089

Product Number

2

Dosage Form

-

Strength

198MG

Approval Date

2019-03-27

Regulatory Status

RX

2019
27 Mar
RX Application: 206089

Drug Name

JATENZO

Product Number

3

Dosage Form

-

Strength

237MG

Approval Date

2019-03-27

206089 / 3

Active Ingredient

TESTOSTERONE UNDECANOATE

Application Number

206089

Product Number

3

Dosage Form

-

Strength

237MG

Approval Date

2019-03-27

Regulatory Status

RX

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Drug Status Breakdown
8 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

ELIGARD KIT

Application Number

21343

Product Number

1

Active Ingredient

LEUPROLIDE ACETATE

Dosage Form

-

Strength

7.5MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

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Reliable Data

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