Avanthi Pharma RX
FDA Approved Drugs

Avanthi 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 14
  • Latest Approval Date Aug 07, 2017
  • Data Source FDA
  • First Approval Date Mar 06, 2009
All
16
View
Discontinued
1
View
OTC
1
View
RX
14
View
Company Overview

Company

Avanthi Pharma RX

Country

U.S.A

Website

Visit Website

Email

info@avanthiinc.com

Social Profiles

Company Snapshot

Avanthi Pharma RX

110 Terry Drive, Suite 100. Newtown, PA 18940

U.S.A

avanthiinc.com/ info@avanthiinc.com View on Map
FDA Approved Drug Records ( 14 records )
2015
23 Nov
RX Application: 203548

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2015-11-23

203548 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

203548

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2015-11-23

Regulatory Status

RX

2015
23 Nov
RX Application: 203548

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2015-11-23

203548 / 2

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

203548

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2015-11-23

Regulatory Status

RX

2010
22 Dec
RX Application: 201212

Drug Name

DIETHYLPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2010-12-22

201212 / 1

Active Ingredient

DIETHYLPROPION HYDROCHLORIDE

Application Number

201212

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2010-12-22

Regulatory Status

RX

2017
07 Aug
RX Application: 207176

Drug Name

HOMATROPINE METHYLBROMIDE AND HYDROCODONE BITARTRATE

Product Number

1

Dosage Form

-

Strength

1.5MG;5MG

Approval Date

2017-08-07

207176 / 1

Active Ingredient

HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE

Application Number

207176

Product Number

1

Dosage Form

-

Strength

1.5MG;5MG

Approval Date

2017-08-07

Regulatory Status

RX

2009
06 Mar
RX Application: 79175

Drug Name

INDOMETHACIN

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2009-03-06

79175 / 1

Active Ingredient

INDOMETHACIN

Application Number

79175

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2009-03-06

Regulatory Status

RX

2016
12 Sep
RX Application: 203495

Drug Name

LOMAIRA

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

2016-09-12

203495 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

203495

Product Number

1

Dosage Form

-

Strength

8MG

Approval Date

2016-09-12

Regulatory Status

RX

2009
31 Aug
RX Application: 91393

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2009-08-31

91393 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

91393

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2009-08-31

Regulatory Status

RX

2009
31 Aug
RX Application: 91393

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2009-08-31

91393 / 2

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

91393

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2009-08-31

Regulatory Status

RX

2009
31 Aug
RX Application: 91393

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2009-08-31

91393 / 3

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

91393

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2009-08-31

Regulatory Status

RX

2009
31 Aug
RX Application: 91393

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2009-08-31

91393 / 4

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

91393

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2009-08-31

Regulatory Status

RX

2009
31 Aug
RX Application: 91393

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2009-08-31

91393 / 5

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

91393

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2009-08-31

Regulatory Status

RX

2015
17 Aug
RX Application: 202773

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2015-08-17

202773 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

202773

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2015-08-17

Regulatory Status

RX

2013
30 Jan
RX Application: 203601

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2013-01-30

203601 / 1

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

203601

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2013-01-30

Regulatory Status

RX

2013
30 Jan
RX Application: 203601

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2013-01-30

203601 / 2

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

203601

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2013-01-30

Regulatory Status

RX

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Drug Status Breakdown
14 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

DEXTROAMPHETAMINE SULFATE

Application Number

203548

Product Number

1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Dosage Form

-

Strength

5MG

FDA Approved Drug Data

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