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Data / Drug companies / Sun Pharmaceutical Industries, Inc.

Sun Pharmaceutical Industries, Inc.: 5 products in the FDA NDC directory, labeler code 45567

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

Sun Pharmaceutical Industries, Inc. (labeler code 45567) lists 5 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 5 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on September 2, 2019.

The request: Watch Sun Pharmaceutical Industries, Inc. (FDA labeler code 45567): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
45567
Products in commercial distribution
5
Packages
8
Finished drugs by generic name
5
Prescription products
5
Over the counter products
0
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 19, 1978
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)360%
Generic drugs (ANDA)240%

Products by type

TypeProductsShare
Prescription drugs5100%

Drugs it lists

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

DrugProductsCompanies listing it
Betiatide11
Technetium tc 99m sulfur colloid11
Kit for the preparation of technetium tc 99m mebrofenin11
Tc 99m medronate11
Technetium tc99m pyrophosphate11

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution360%
Kit120%
Injection120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Kit for the Preparation of Technetium Tc99m Mertiatide45567-0655Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 2, 2019
Kit for the Preparation of Technetium Tc 99m Mebrofenin45567-0455Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 29, 2008
Kit for the Preparation of Technetium Tc99m Pyrophosphate45567-0060InjectionNew drug applications (NDA)June 30, 1987
Kit for the Preparation of Technetium Tc 99M Medronate45567-0040Injection, powder, lyophilized, for solutionNew drug applications (NDA)August 29, 1979
Kit for the Prepartion of Technetium Tc99m Sulfur Colloid45567-0030KitNew drug applications (NDA)April 19, 1978

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.