Vivus
FDA Approved Drugs

Vivus

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 7
  • Latest Approval Date Jul 17, 2012
  • Data Source FDA
  • First Approval Date Apr 27, 2012
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Company

Vivus

Country

U.S.A

Email

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Company Snapshot

Vivus

900 E. Hamilton Avenue, Suite 550, Campbell, CA 95008

U.S.A

www.vivus.com/ View on Map
FDA Approved Drug Records ( 7 records )
2012
17 Jul
RX Application: 22580

Drug Name

QSYMIA

Product Number

1

Dosage Form

-

Strength

EQ 3.75MG BASE;23MG

Approval Date

2012-07-17

22580 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

Application Number

22580

Product Number

1

Dosage Form

-

Strength

EQ 3.75MG BASE;23MG

Approval Date

2012-07-17

Regulatory Status

RX

2012
17 Jul
RX Application: 22580

Drug Name

QSYMIA

Product Number

2

Dosage Form

-

Strength

EQ 7.5MG BASE;46MG

Approval Date

2012-07-17

22580 / 2

Active Ingredient

PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

Application Number

22580

Product Number

2

Dosage Form

-

Strength

EQ 7.5MG BASE;46MG

Approval Date

2012-07-17

Regulatory Status

RX

2012
17 Jul
RX Application: 22580

Drug Name

QSYMIA

Product Number

3

Dosage Form

-

Strength

EQ 11.25MG BASE;69MG

Approval Date

2012-07-17

22580 / 3

Active Ingredient

PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

Application Number

22580

Product Number

3

Dosage Form

-

Strength

EQ 11.25MG BASE;69MG

Approval Date

2012-07-17

Regulatory Status

RX

2012
17 Jul
RX Application: 22580

Drug Name

QSYMIA

Product Number

4

Dosage Form

-

Strength

EQ 15MG BASE;92MG

Approval Date

2012-07-17

22580 / 4

Active Ingredient

PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

Application Number

22580

Product Number

4

Dosage Form

-

Strength

EQ 15MG BASE;92MG

Approval Date

2012-07-17

Regulatory Status

RX

2012
27 Apr
RX Application: 202276

Drug Name

STENDRA

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2012-04-27

202276 / 1

Active Ingredient

AVANAFIL

Application Number

202276

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2012-04-27

Regulatory Status

RX

2012
27 Apr
RX Application: 202276

Drug Name

STENDRA

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2012-04-27

202276 / 2

Active Ingredient

AVANAFIL

Application Number

202276

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2012-04-27

Regulatory Status

RX

2012
27 Apr
RX Application: 202276

Drug Name

STENDRA

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2012-04-27

202276 / 3

Active Ingredient

AVANAFIL

Application Number

202276

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2012-04-27

Regulatory Status

RX

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Drug Status Breakdown
7 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

QSYMIA

Application Number

22580

Product Number

1

Active Ingredient

PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

Dosage Form

-

Strength

EQ 3.75MG BASE;23MG

FDA Approved Drug Data

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