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Data / Drug companies / Hainan Shuangcheng Pharmaceuticals Co., Ltd.

Hainan Shuangcheng Pharmaceuticals Co., Ltd.: 8 products in the FDA NDC directory, labeler code 52958

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

Hainan Shuangcheng Pharmaceuticals Co., Ltd. (labeler code 52958) lists 8 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 4 bulk ingredients, 4 prescription drugs. Its main marketing category is bulk ingredients. The newest product started marketing on December 17, 2025.

The request: Watch Hainan Shuangcheng Pharmaceuticals Co., Ltd. (FDA labeler code 52958): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
52958
Products in commercial distribution
8
Packages
8
Finished drugs by generic name
3
Prescription products
4
Over the counter products
0
Flagged as original packager
4 of 4 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
July 31, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients450%
Generic drugs (ANDA)450%

Products by type

TypeProductsShare
Bulk ingredients450%
Prescription drugs450%

Drugs it lists

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

DrugProductsCompanies listing it
Eptifibatide29
Octreotide acetate111
Bivalirudin113

Dosage forms

Dosage formProductsShare
Powder450%
Injection, solution337.5%
Injection, powder, lyophilized, for solution112.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Bortezomib52958-134PowderBulk ingredientsDecember 17, 2025
Octreotide acetate52958-117PowderBulk ingredientsMay 2, 2024
Octreotide acetate52958-046Injection, solutionGeneric drugs (ANDA)May 2, 2024
Eptifibatide52958-040Injection, solutionGeneric drugs (ANDA)April 21, 2022
Eptifibatide52958-402Injection, solutionGeneric drugs (ANDA)September 7, 2021
Bivalirudin52958-112PowderBulk ingredientsOctober 28, 2019
Bivalirudin52958-034Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)October 23, 2019
Eptifibatide52958-001PowderBulk ingredientsJuly 31, 2012

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.