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Data / Drug companies / Medi-Physics Inc. DBA GE Healthcare

Medi-Physics Inc. DBA GE Healthcare: 11 products in the FDA NDC directory, labeler code 17156

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

Medi-Physics Inc. DBA GE Healthcare (labeler code 17156) lists 11 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 9 prescription drugs, 2 bulk ingredients. Its main marketing category is new drug applications (NDA). The newest product started marketing on September 25, 2018.

The request: Watch Medi-Physics Inc. DBA GE Healthcare (FDA labeler code 17156): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
17156
Products in commercial distribution
11
Packages
11
Finished drugs by generic name
8
Prescription products
9
Over the counter products
0
Flagged as original packager
9 of 9 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
February 18, 1982
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)981.8%
Bulk ingredients218.2%

Products by type

TypeProductsShare
Prescription drugs981.8%
Bulk ingredients218.2%

Drugs it lists

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

DrugProductsCompanies listing it
Tetrofosmin21
Technetium tc-99m exametazime and cobaltous chloride11
Flutemetamol f-1811
Iobenguane i-12311
Indium in-111 oxyquinoline12
Indium in-111 pentetate disodium11
Ioflupane i-12312
Technetium tc-99m exametazime11

Dosage forms

Dosage formProductsShare
Solution545.5%
Injection, powder, lyophilized, for solution327.3%
Kit19.1%
Injection19.1%
Injection, solution19.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ceretec17156-025KitNew drug applications (NDA)September 25, 2018
Vizamyl17156-067SolutionNew drug applications (NDA)January 1, 2014
Sodium thiosulfate17156-946SolutionBulk ingredientsJuly 1, 2013
Sodium iodide i-12317156-945SolutionBulk ingredientsJuly 1, 2013
DaTscan17156-210Injection, solutionNew drug applications (NDA)March 1, 2011
Myoview17156-026Injection, powder, lyophilized, for solutionNew drug applications (NDA)February 26, 2009
AdreView17156-235InjectionNew drug applications (NDA)September 19, 2008
Myoview17156-024Injection, powder, lyophilized, for solutionNew drug applications (NDA)February 9, 1996
Ceretec17156-022Injection, powder, lyophilized, for solutionNew drug applications (NDA)December 30, 1988
Indium in 111 Oxyquinoline17156-021SolutionNew drug applications (NDA)December 1, 1985
Indium DTPA In 11117156-251SolutionNew drug applications (NDA)February 18, 1982

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.