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Data / Drug companies / Zhejiang Lepu Pharmaceutical Co., Ltd.

Zhejiang Lepu Pharmaceutical Co., Ltd.: 10 products in the FDA NDC directory, labeler code 68578

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

Zhejiang Lepu Pharmaceutical Co., Ltd. (labeler code 68578) lists 10 products in the FDA National Drug Code Directory. By type: 10 bulk ingredients. Its main marketing category is bulk ingredients for compounding. The newest product started marketing on September 27, 2023.

The request: Watch Zhejiang Lepu Pharmaceutical Co., Ltd. (FDA labeler code 68578): 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
68578
Products in commercial distribution
10
Packages
15
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
December 30, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients for compounding660%
Bulk ingredients440%

Products by type

TypeProductsShare
Bulk ingredients10100%

Dosage forms

Dosage formProductsShare
Powder10100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Vortioxetine hydrobromide68578-0020PowderBulk ingredients for compoundingSeptember 27, 2023
Ponatinib hydrochloride68578-0016PowderBulk ingredients for compoundingOctober 13, 2022
Azelastine hydrochloride68578-0017PowderBulk ingredients for compoundingDecember 15, 2021
Pazopanib hydrochloride68578-0015PowderBulk ingredients for compoundingSeptember 15, 2021
Clopidogrel bisulfate68578-0014PowderBulk ingredientsNovember 18, 2020
Idelalisib68578-0013PowderBulk ingredients for compoundingMay 16, 2018
Macitentan68578-0019PowderBulk ingredients for compoundingMay 31, 2017
Linezolid68578-0009PowderBulk ingredientsDecember 30, 2013
Rosuvastatin calcium68578-0011PowderBulk ingredientsJanuary 16, 2013
Atorvastatin calcium trihydrate68578-0010PowderBulk ingredientsDecember 30, 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.