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Data / Drug companies / Shandong Xinhua Pharmaceutical Company Limited

Shandong Xinhua Pharmaceutical Company Limited: 63 products in the FDA NDC directory, labeler code 58624

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

Shandong Xinhua Pharmaceutical Company Limited (labeler code 58624) lists 63 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 51 bulk ingredients, 10 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on January 19, 2026.

The request: Watch Shandong Xinhua Pharmaceutical Company Limited (FDA labeler code 58624): 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
58624
Products in commercial distribution
63
Packages
70
Finished drugs by generic name
2
Prescription products
1
Over the counter products
1
Controlled substance products
Schedule IV 2
Flagged as original packager
2 of 2 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
October 1, 1983
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients5181%
Drugs for further processing1015.9%
Generic drugs (ANDA)11.6%
Over the counter monograph drugs11.6%

Products by type

TypeProductsShare
Bulk ingredients5181%
Drugs for further processing1015.9%
Prescription drugs11.6%
Over the counter drugs11.6%

Drugs it lists

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

DrugProductsCompanies listing it
Sevelamer carbonate135
Calcium polycarbophil133

Dosage forms

Dosage formProductsShare
Powder4876.2%
Tablet, film coated812.7%
Tablet, coated46.3%
Liquid23.2%
Poultice11.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Phosphate Binder1

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Theophylline anhydrous58624-0713PowderBulk ingredientsJanuary 19, 2026
Ibuprofen58624-6004Tablet, coatedDrugs for further processingFebruary 28, 2025
Sevelamer carbonate58624-5001Tablet, film coatedGeneric drugs (ANDA)February 27, 2025
Omega-3-acid ethyl esters58624-0712LiquidBulk ingredientsAugust 26, 2024
Bismuth subsalicylate58624-0711PowderBulk ingredientsAugust 22, 2024
Hydrocortisone acetate58624-0710PowderBulk ingredientsMay 9, 2024
Sevelamer carbonate58624-0709PowderBulk ingredientsMay 9, 2024
Glimepiride58624-0708PowderBulk ingredientsMay 9, 2024
Metamizole sodium monohydrate58624-0707PowderBulk ingredientsMarch 28, 2024
Calcium Polycarbophil58624-5003Tablet, film coatedOver the counter monograph drugsApril 12, 2023
Ibuprofen58624-7006Tablet, film coatedDrugs for further processingJune 16, 2021
Ibuprofen58624-7005Tablet, film coatedDrugs for further processingJune 16, 2021
Ibuprofen58624-7004Tablet, film coatedDrugs for further processingJune 16, 2021
Ibuprofen58624-7003Tablet, film coatedDrugs for further processingJune 16, 2021
Ibuprofen58624-7002Tablet, film coatedDrugs for further processingJune 16, 2021
Ibuprofen58624-7001Tablet, film coatedDrugs for further processingJune 16, 2021
Ethyl icosapentate58624-0411LiquidBulk ingredientsMay 24, 2021
Ibuprofen58624-6003Tablet, coatedDrugs for further processingOctober 5, 2020
Ibuprofen58624-6002Tablet, coatedDrugs for further processingOctober 5, 2020
Ibuprofen58624-6001Tablet, coatedDrugs for further processingOctober 5, 2020
Ibuprofen sodium58624-0536PowderBulk ingredientsJune 11, 2010
Nimodipine58624-0495PowderBulk ingredientsApril 7, 2008
Antipyrine58624-0620PowderBulk ingredientsJanuary 1, 2008
Meloxicam58624-0430PowderBulk ingredientsJanuary 1, 2007
Tramadol hydrochloride58624-0201PowderBulk ingredientsJanuary 1, 2003

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.