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Data / Drug companies / Fosun Pharma USA Inc.

Fosun Pharma USA Inc.: 55 products in the FDA NDC directory, labeler code 72266

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

Fosun Pharma USA Inc. (labeler code 72266) lists 55 products in the FDA National Drug Code Directory, covering 36 finished drugs by generic name. By type: 55 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 29, 2026.

The request: Watch Fosun Pharma USA Inc. (FDA labeler code 72266): 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
72266
Products in commercial distribution
55
Packages
58
Finished drugs by generic name
36
Prescription products
55
Over the counter products
0
Controlled substance products
Schedule V 1
Flagged as original packager
55 of 55 products that carry the flag
Started marketing in the last 12 months
7
Earliest marketing start
March 18, 2019
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)5396.4%
New drug applications (NDA)23.6%

Products by type

TypeProductsShare
Prescription drugs55100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution1425.5%
Injection, powder, lyophilized, for solution1323.6%
Injection1120%
Solution/ drops610.9%
Tablet, extended release47.3%
Solution47.3%
Solution, gel forming / drops23.6%
Kit11.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sugammadex72266-269Injection, solutionGeneric drugs (ANDA)July 29, 2026
Sugammadex72266-268Injection, solutionGeneric drugs (ANDA)July 29, 2026
Guanfacine72266-258Tablet, extended releaseGeneric drugs (ANDA)April 3, 2026
Bupivacaine Hydrochloride72266-264Injection, solutionGeneric drugs (ANDA)February 6, 2026
Bupivacaine Hydrochloride72266-263Injection, solutionGeneric drugs (ANDA)February 6, 2026
Thiamine Hydrochloride72266-260Injection, solutionGeneric drugs (ANDA)February 6, 2026
Bimatoprost72266-241Solution/ dropsGeneric drugs (ANDA)November 30, 2025
Guanfacine72266-257Tablet, extended releaseGeneric drugs (ANDA)October 1, 2025
Guanfacine72266-256Tablet, extended releaseGeneric drugs (ANDA)October 1, 2025
Guanfacine72266-255Tablet, extended releaseGeneric drugs (ANDA)October 1, 2025
Levothyroxine Sodium72266-261Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 16, 2025
Arformoterol tartrate72266-259SolutionGeneric drugs (ANDA)April 8, 2025
Polymyxin b72266-249Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)August 31, 2023
Cisplatin72266-253Injection, solutionGeneric drugs (ANDA)August 11, 2023
Cisplatin72266-252Injection, solutionGeneric drugs (ANDA)August 11, 2023
Ketorolac tromethamine72266-234Injection, solutionGeneric drugs (ANDA)June 23, 2023
Ketorolac tromethamine72266-119Injection, solutionGeneric drugs (ANDA)June 23, 2023
Ketorolac tromethamine72266-118Injection, solutionGeneric drugs (ANDA)June 23, 2023
Calcitriol72266-251InjectionGeneric drugs (ANDA)June 20, 2023
Zoledronic acid72266-152InjectionGeneric drugs (ANDA)June 12, 2023
Prochlorperazine Edisylate72266-204InjectionGeneric drugs (ANDA)May 1, 2023
Doxycycline72266-237Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 12, 2023
Timolol Maleate Ophthalmic Gel Forming Solution72266-200Solution, gel forming / dropsGeneric drugs (ANDA)March 15, 2023
Dorzolamide Hydrochloride72266-197SolutionGeneric drugs (ANDA)January 23, 2023
Sincalide72266-248Injection, powder, lyophilized, for solutionNew drug applications (NDA)January 9, 2023

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.