KREITCHMAN PET CENTER
FDA Approved Drugs

KREITCHMAN PET CENTER

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 3
  • Latest Approval Date May 19, 2016
  • Data Source FDA
  • First Approval Date Dec 09, 2013
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KREITCHMAN PET CENTER

Country

U.S.A

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KREITCHMAN PET CENTER

U.S.A

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FDA Approved Drug Records ( 3 records )
2013
09 Dec
RX Application: 203938

Drug Name

AMMONIA N 13

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2013-12-09

203938 / 1

Active Ingredient

AMMONIA N-13

Application Number

203938

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2013-12-09

Regulatory Status

RX

2016
11 Apr
RX Application: 203942

Drug Name

FLUDEOXYGLUCOSE F18

Product Number

1

Dosage Form

-

Strength

10-100mCi/ML

Approval Date

2016-04-11

203942 / 1

Active Ingredient

FLUDEOXYGLUCOSE F-18

Application Number

203942

Product Number

1

Dosage Form

-

Strength

10-100mCi/ML

Approval Date

2016-04-11

Regulatory Status

RX

2016
19 May
RX Application: 203936

Drug Name

SODIUM FLUORIDE F-18

Product Number

1

Dosage Form

-

Strength

10-200mCi/ML

Approval Date

2016-05-19

203936 / 1

Active Ingredient

SODIUM FLUORIDE F-18

Application Number

203936

Product Number

1

Dosage Form

-

Strength

10-200mCi/ML

Approval Date

2016-05-19

Regulatory Status

RX

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Drug Status Breakdown
3 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

203938

Product Number

1

Active Ingredient

AMMONIA N-13

Dosage Form

-

Strength

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

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