UCSF RODIOPHARM
FDA Approved Drugs

UCSF RODIOPHARM

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 Discontinued
  • Total Records 4
  • Latest Approval Date Nov 20, 2017
  • Data Source FDA
  • First Approval Date Mar 13, 2014
All
4
View
Discontinued
2
View
RX
2
View
Company Overview

Company

UCSF RODIOPHARM

Country

U.S.A

Email

Social Profiles

Company Snapshot

UCSF RODIOPHARM

Parnassus 505 Parnassus Ave. San Francisco, CA 94143

U.S.A

radiology.ucsf.edu/ View on Map
FDA Approved Drug Records ( 4 records )
2014
28 Mar
RX Application: 204496

Drug Name

AMMONIA N 13

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2014-03-28

204496 / 1

Active Ingredient

AMMONIA N-13

Application Number

204496

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2014-03-28

Regulatory Status

RX

2017
20 Nov
Discontinued Application: 208444

Drug Name

CHOLINE C-11

Product Number

1

Dosage Form

-

Strength

4-33.1mCi/ML

Approval Date

2017-11-20

208444 / 1

Active Ingredient

CHOLINE C-11

Application Number

208444

Product Number

1

Dosage Form

-

Strength

4-33.1mCi/ML

Approval Date

2017-11-20

Regulatory Status

Discontinued

2014
09 May
RX Application: 203902

Drug Name

FLUDEOXYGLUCOSE F18

Product Number

1

Dosage Form

-

Strength

20-300mCi/ML

Approval Date

2014-05-09

203902 / 1

Active Ingredient

FLUDEOXYGLUCOSE F-18

Application Number

203902

Product Number

1

Dosage Form

-

Strength

20-300mCi/ML

Approval Date

2014-05-09

Regulatory Status

RX

2014
13 Mar
Discontinued Application: 204437

Drug Name

SODIUM FLUORIDE F-18

Product Number

1

Dosage Form

-

Strength

10-200mCi/ML

Approval Date

2014-03-13

204437 / 1

Active Ingredient

SODIUM FLUORIDE F-18

Application Number

204437

Product Number

1

Dosage Form

-

Strength

10-200mCi/ML

Approval Date

2014-03-13

Regulatory Status

Discontinued

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Drug Status Breakdown
4 total
  • RX
  • Discontinued
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

AMMONIA N 13

Application Number

204496

Product Number

1

Active Ingredient

AMMONIA N-13

Dosage Form

-

Strength

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

FDA Approved Drug Data

Approved drug product information

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