APIL RX
FDA Approved Drugs

APIL 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 5
  • Latest Approval Date Apr 19, 2013
  • Data Source FDA
  • First Approval Date May 25, 2002
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30
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Discontinued
25
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RX
5
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APIL RX

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FDA Approved Drug Records ( 5 records )
2002
25 May
RX Application: 20835

Drug Name

ACTONEL

Product Number

3

Dosage Form

-

Strength

35MG

Approval Date

2002-05-25

20835 / 3

Active Ingredient

RISEDRONATE SODIUM

Application Number

20835

Product Number

3

Dosage Form

-

Strength

35MG

Approval Date

2002-05-25

Regulatory Status

RX

2008
22 Apr
RX Application: 20835

Drug Name

ACTONEL

Product Number

5

Dosage Form

-

Strength

150MG

Approval Date

2008-04-22

20835 / 5

Active Ingredient

RISEDRONATE SODIUM

Application Number

20835

Product Number

5

Dosage Form

-

Strength

150MG

Approval Date

2008-04-22

Regulatory Status

RX

2010
08 Oct
RX Application: 22560

Drug Name

ATELVIA

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

2010-10-08

22560 / 1

Active Ingredient

RISEDRONATE SODIUM

Application Number

22560

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

2010-10-08

Regulatory Status

RX

2010
21 Oct
RX Application: 22501

Drug Name

LO LOESTRIN FE

Product Number

1

Dosage Form

-

Strength

0.01MG,0.01MG;1MG,N/A

Approval Date

2010-10-21

22501 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

22501

Product Number

1

Dosage Form

-

Strength

0.01MG,0.01MG;1MG,N/A

Approval Date

2010-10-21

Regulatory Status

RX

2013
19 Apr
RX Application: 204426

Drug Name

TAYTULLA

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2013-04-19

204426 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

204426

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2013-04-19

Regulatory Status

RX

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Drug Status Breakdown
5 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

ACTONEL

Application Number

20835

Product Number

3

Active Ingredient

RISEDRONATE SODIUM

Dosage Form

-

Strength

35MG

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