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01 2Biophore India Pharmaceuticals Pvt Ltd

02 1ANDA Repository

03 1Amphastar Pharmaceuticals

04 1Annora Pharma

05 13Bayer AG

06 15Bracco

07 6GE Healthcare Inc

08 2Jodas Expoim Pvt. Ltd

09 4Mallinckrodt Pharmaceuticals

10 2ORIFARM GROUP AS

11 1Xian Libang Pharmaceutical Co.,Ltd

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

Regulatory Info :

Registration Country : India

Diatrizoate Meglumine

Brand Name :

Dosage Form : Injection

Dosage Strength : 60%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Biophore

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

Regulatory Info :

Registration Country : India

Diatrizoate Sodium; Diatrizoate Meglumine

Brand Name :

Dosage Form : Injection

Dosage Strength :

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Biophore

03

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : ANGIOVIST 370

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-09-23

Application Number : 87723

Regulatory Info : DISCN

Registration Country : USA

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04

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : ANGIOVIST 292

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 52%;8%

Packaging :

Approval Date : 1982-09-23

Application Number : 87724

Regulatory Info : DISCN

Registration Country : USA

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05

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : ANGIOVIST 282

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 60%

Packaging :

Approval Date : 1982-09-23

Application Number : 87726

Regulatory Info : DISCN

Registration Country : USA

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06

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : GASTROVIST

Dosage Form : SOLUTION;ORAL, RECTAL

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-09-23

Application Number : 87728

Regulatory Info : DISCN

Registration Country : USA

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07

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : UROVIST CYSTO

Dosage Form : SOLUTION;URETERAL

Dosage Strength : 30%

Packaging :

Approval Date : 1982-09-23

Application Number : 87729

Regulatory Info : DISCN

Registration Country : USA

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08

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : RENOGRAFIN-76

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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09

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : RENOGRAFIN-60

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 52%;8%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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10

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : RENO-DIP

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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11

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : RENO-60

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 60%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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12

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : DIATRIZOATE MEGLUMINE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 76%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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13

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : CYSTOGRAFIN

Dosage Form : SOLUTION;URETHRAL

Dosage Strength : 30%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : RX

Registration Country : USA

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14

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : RENOVIST II

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 28.5%;29.1%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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15

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : RENOVIST

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 34.3%;35%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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16

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : RENO-30

Dosage Form : SOLUTION;URETERAL

Dosage Strength : 30%

Packaging :

Approval Date : 1982-01-01

Application Number : 10040

Regulatory Info : DISCN

Registration Country : USA

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17

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : CYSTOGRAFIN DILUTE

Dosage Form : SOLUTION;URETHRAL

Dosage Strength : 18%

Packaging :

Approval Date : 1982-11-09

Application Number : 10040

Regulatory Info : RX

Registration Country : USA

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18

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : GASTROGRAFIN

Dosage Form : SOLUTION;ORAL, RECTAL

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-01-01

Application Number : 11245

Regulatory Info : RX

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; IODIPAMIDE MEGLUMINE

Brand Name : SINOGRAFIN

Dosage Form : SOLUTION;INTRAUTERINE

Dosage Strength : 52.7%;26.8%

Packaging :

Approval Date : 1982-01-01

Application Number : 11324

Regulatory Info : DISCN

Registration Country : USA

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20

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : CARDIOGRAFIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 85%

Packaging :

Approval Date : 1982-01-01

Application Number : 11620

Regulatory Info : DISCN

Registration Country : USA

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21

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : HYPAQUE-M,90%

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 60%;30%

Packaging :

Approval Date : 1982-01-01

Application Number : 10220

Regulatory Info : DISCN

Registration Country : USA

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22

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : HYPAQUE-M,75%

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50%;25%

Packaging :

Approval Date : 1982-01-01

Application Number : 10220

Regulatory Info : DISCN

Registration Country : USA

blank

23

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : HYPAQUE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 60%

Packaging :

Approval Date : 1982-01-01

Application Number : 16403

Regulatory Info : DISCN

Registration Country : USA

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24

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : HYPAQUE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30%

Packaging :

Approval Date : 1982-01-01

Application Number : 16403

Regulatory Info : DISCN

Registration Country : USA

blank

25

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE

Brand Name : HYPAQUE-CYSTO

Dosage Form : SOLUTION;URETHRAL

Dosage Strength : 30%

Packaging :

Approval Date : 1982-01-01

Application Number : 16403

Regulatory Info : DISCN

Registration Country : USA

blank

26

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : HYPAQUE-76

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-01-01

Application Number : 86505

Regulatory Info : DISCN

Registration Country : USA

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27

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : MD-76R

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1989-09-29

Application Number : 19292

Regulatory Info : DISCN

Registration Country : USA

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28

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : MD-76

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-01-01

Application Number : 87073

Regulatory Info : DISCN

Registration Country : USA

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29

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : MD-60

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 52%;8%

Packaging :

Approval Date : 1982-01-01

Application Number : 87074

Regulatory Info : DISCN

Registration Country : USA

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30

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Brand Name : MD-GASTROVIEW

Dosage Form : SOLUTION;ORAL, RECTAL

Dosage Strength : 66%;10%

Packaging :

Approval Date : 1982-01-01

Application Number : 87388

Regulatory Info : RX

Registration Country : USA

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