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Data / Drug companies / Bracco Diagnostics Inc

Bracco Diagnostics Inc: 36 products in the FDA NDC directory, labeler code 0270

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Bracco Diagnostics Inc (labeler code 0270) lists 36 products in the FDA National Drug Code Directory, covering 11 finished drugs by generic name. By type: 36 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on January 1, 2026.

The request: Watch Bracco Diagnostics Inc (FDA labeler code 0270): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0270
Products in commercial distribution
36
Packages
69
Finished drugs by generic name
11
Prescription products
36
Over the counter products
0
Flagged as original packager
32 of 32 products that carry the flag
Started marketing in the last 12 months
2
Earliest marketing start
February 26, 1958
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)2980.6%
Unapproved drugs for a shortage719.4%

Products by type

TypeProductsShare
Prescription drugs36100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Iomeprol injection92
Iopamidol82
Gadopiclenol52
Sulfur hexafluoride41
Gadoteridol22
Gadobenate dimeglumine21
Diatrizoate meglumine21
Rubidium chloride rb-8211
Mebrofenin11
Diatrizoate meglumine and diatrizoate sodium14
Sincalide14

Dosage forms

Dosage formProductsShare
Injection, solution2466.7%
Injection513.9%
Injection, powder, lyophilized, for suspension25.6%
Kit25.6%
Injection, powder, lyophilized, for solution25.6%
Liquid12.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Iomervu0270-7018Injection, solutionNew drug applications (NDA)January 1, 2026
Iomervu0270-7017Injection, solutionNew drug applications (NDA)January 1, 2026
Vueway0270-7035InjectionNew drug applications (NDA)September 21, 2022
Vueway0270-7030InjectionNew drug applications (NDA)September 21, 2022
Vueway0270-7025InjectionNew drug applications (NDA)September 21, 2022
Vueway0270-7020InjectionNew drug applications (NDA)September 21, 2022
Vueway0270-7015InjectionNew drug applications (NDA)September 21, 2022
Iomeron0270-9400Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Iomeron0270-9350Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Iomeron0270-9300Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Iomeron0270-7400Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Iomeron0270-7350Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Iomeron0270-7300Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Iomeron0270-7250Injection, solutionUnapproved drugs for a shortageJuly 1, 2022
Lumason0270-7097Injection, powder, lyophilized, for suspensionNew drug applications (NDA)April 1, 2021
LumaSon0270-7097Injection, powder, lyophilized, for suspensionNew drug applications (NDA)April 1, 2021
LumaSon0270-7099KitNew drug applications (NDA)January 15, 2020
LumaSon0270-7099KitNew drug applications (NDA)January 15, 2015
Isovue 3700270-1316Injection, solutionNew drug applications (NDA)June 20, 2014
Isovue 3000270-1315Injection, solutionNew drug applications (NDA)June 20, 2014
MultiHance0270-5264Injection, solutionNew drug applications (NDA)November 23, 2004
MultiHance0270-5164Injection, solutionNew drug applications (NDA)November 23, 2004
ProHance0270-1111Injection, solutionNew drug applications (NDA)October 9, 2003
ProHance0270-1111Injection, solutionNew drug applications (NDA)November 16, 1992
CardioGen-820270-0091Injection, solutionNew drug applications (NDA)December 30, 1989

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.