Avet Pharmaceuticals
FDA Approved Drugs

Avet Pharmaceuticals

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 RX
  • Total Records 14
  • Latest Approval Date Oct 13, 2017
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
14
View
Discontinued
7
View
RX
7
View
Company Overview

Company

Avet Pharmaceuticals

Country

U.S.A

Website

Visit Website

Email

bd@Avetpharma.com

Social Profiles

LinkedIn
Company Snapshot

Avet Pharmaceuticals

One Tower Center Blvd, Suite 1700, East Brunswick Township, New Jersey 08816, US

U.S.A

avetpharma.com/ bd@Avetpharma.com View on Map
FDA Approved Drug Records ( 14 records )
2008
17 Oct
Discontinued Application: 78489

Drug Name

ALPRAZOLAM

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2008-10-17

78489 / 1

Active Ingredient

ALPRAZOLAM

Application Number

78489

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2008-10-17

Regulatory Status

Discontinued

2008
17 Oct
Discontinued Application: 78489

Drug Name

ALPRAZOLAM

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2008-10-17

78489 / 2

Active Ingredient

ALPRAZOLAM

Application Number

78489

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2008-10-17

Regulatory Status

Discontinued

2008
17 Oct
Discontinued Application: 78489

Drug Name

ALPRAZOLAM

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2008-10-17

78489 / 3

Active Ingredient

ALPRAZOLAM

Application Number

78489

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2008-10-17

Regulatory Status

Discontinued

2008
17 Oct
Discontinued Application: 78489

Drug Name

ALPRAZOLAM

Product Number

4

Dosage Form

-

Strength

3MG

Approval Date

2008-10-17

78489 / 4

Active Ingredient

ALPRAZOLAM

Application Number

78489

Product Number

4

Dosage Form

-

Strength

3MG

Approval Date

2008-10-17

Regulatory Status

Discontinued

2015
29 Jun
RX Application: 202315

Drug Name

CALCIUM ACETATE

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2015-06-29

202315 / 1

Active Ingredient

CALCIUM ACETATE

Application Number

202315

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2015-06-29

Regulatory Status

RX

2015
22 Jan
RX Application: 202885

Drug Name

CALCIUM ACETATE

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2015-01-22

202885 / 1

Active Ingredient

CALCIUM ACETATE

Application Number

202885

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2015-01-22

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 80530

Drug Name

DOLENE

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

80530 / 1

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

80530

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2017
13 Oct
Discontinued Application: 207935

Drug Name

DUTASTERIDE

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2017-10-13

207935 / 1

Active Ingredient

DUTASTERIDE

Application Number

207935

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2017-10-13

Regulatory Status

Discontinued

2012
25 Sep
Discontinued Application: 200892

Drug Name

ETHOSUXIMIDE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2012-09-25

200892 / 1

Active Ingredient

ETHOSUXIMIDE

Application Number

200892

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2012-09-25

Regulatory Status

Discontinued

2010
26 Feb
RX Application: 40858

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2010-02-26

40858 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

40858

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2010-02-26

Regulatory Status

RX

2010
26 Feb
RX Application: 40858

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2010-02-26

40858 / 2

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

40858

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2010-02-26

Regulatory Status

RX

2010
26 Feb
RX Application: 40858

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2010-02-26

40858 / 3

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

40858

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2010-02-26

Regulatory Status

RX

2010
26 Feb
RX Application: 40858

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2010-02-26

40858 / 4

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

40858

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2010-02-26

Regulatory Status

RX

2016
30 Aug
RX Application: 204945

Drug Name

TROSPIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2016-08-30

204945 / 1

Active Ingredient

TROSPIUM CHLORIDE

Application Number

204945

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2016-08-30

Regulatory Status

RX

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Drug Status Breakdown
14 total
  • Discontinued
  • 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

ALPRAZOLAM

Application Number

78489

Product Number

1

Active Ingredient

ALPRAZOLAM

Dosage Form

-

Strength

0.5MG

FDA Approved Drug Data

Approved drug product information

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