MCPRF
FDA Approved Drugs

MCPRF

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 4
  • Latest Approval Date Aug 05, 2013
  • Data Source FDA
  • First Approval Date Sep 12, 2012
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FDA Approved Drug Records ( 4 records )
2013
25 Feb
RX Application: 203321

Drug Name

AMMONIA N 13

Product Number

1

Dosage Form

-

Strength

30mCi-300mCi/8ML (3.75-37.5mCi/ML)

Approval Date

2013-02-25

203321 / 1

Active Ingredient

AMMONIA N-13

Application Number

203321

Product Number

1

Dosage Form

-

Strength

30mCi-300mCi/8ML (3.75-37.5mCi/ML)

Approval Date

2013-02-25

Regulatory Status

RX

2012
12 Sep
RX Application: 203155

Drug Name

CHOLINE C-11

Product Number

1

Dosage Form

-

Strength

4-33.1mCi/ML

Approval Date

2012-09-12

203155 / 1

Active Ingredient

CHOLINE C-11

Application Number

203155

Product Number

1

Dosage Form

-

Strength

4-33.1mCi/ML

Approval Date

2012-09-12

Regulatory Status

RX

2013
05 Aug
RX Application: 203612

Drug Name

FLUDEOXYGLUCOSE F18

Product Number

1

Dosage Form

-

Strength

20-240mCi/ML

Approval Date

2013-08-05

203612 / 1

Active Ingredient

FLUDEOXYGLUCOSE F-18

Application Number

203612

Product Number

1

Dosage Form

-

Strength

20-240mCi/ML

Approval Date

2013-08-05

Regulatory Status

RX

2013
28 Jun
RX Application: 203605

Drug Name

SODIUM FLUORIDE F-18

Product Number

1

Dosage Form

-

Strength

10-91.5mCi/ML

Approval Date

2013-06-28

203605 / 1

Active Ingredient

SODIUM FLUORIDE F-18

Application Number

203605

Product Number

1

Dosage Form

-

Strength

10-91.5mCi/ML

Approval Date

2013-06-28

Regulatory Status

RX

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Drug Status Breakdown
4 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

AMMONIA N 13

Application Number

203321

Product Number

1

Active Ingredient

AMMONIA N-13

Dosage Form

-

Strength

30mCi-300mCi/8ML (3.75-37.5mCi/ML)

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