Skip to the page

Data / Drug companies / Bushu Pharmaceuticals, Ltd.

Bushu Pharmaceuticals, Ltd.: 11 products in the FDA NDC directory, labeler code 51148

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

Bushu Pharmaceuticals, Ltd. (labeler code 51148) lists 11 products in the FDA National Drug Code Directory. By type: 11 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on July 3, 2023.

The request: Watch Bushu Pharmaceuticals, Ltd. (FDA labeler code 51148): 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
51148
Products in commercial distribution
11
Packages
11
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
May 10, 1995
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing11100%

Products by type

TypeProductsShare
Drugs for further processing11100%

Dosage forms

Dosage formProductsShare
Tablet, film coated981.8%
Capsule, delayed release19.1%
Tablet, delayed release19.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Fezolinetant51148-014Tablet, film coatedDrugs for further processingJuly 3, 2023
Relugolix51148-013Tablet, film coatedDrugs for further processingDecember 18, 2020
Rufinamide51148-008Tablet, film coatedDrugs for further processingMay 1, 2015
Lurasidone hydrochloride51148-003Tablet, film coatedDrugs for further processingApril 26, 2012
Lurasidone hydrochloride51148-004Tablet, film coatedDrugs for further processingDecember 7, 2011
Lurasidone hydrochloride51148-002Tablet, film coatedDrugs for further processingOctober 28, 2010
Lurasidone hydrochloride51148-001Tablet, film coatedDrugs for further processingOctober 28, 2010
Rufinamide51148-010Tablet, film coatedDrugs for further processingNovember 14, 2008
Rufinamide51148-009Tablet, film coatedDrugs for further processingNovember 14, 2008
Rabeprazole sodium tablets51148-007Tablet, delayed releaseDrugs for further processingAugust 19, 1999
Prevacid capsule 30mg51148-015Capsule, delayed releaseDrugs for further processingMay 10, 1995

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.