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Data / Drug companies / Yung Zip Chemical Industrial Co., LTD.

Yung Zip Chemical Industrial Co., LTD.: 10 products in the FDA NDC directory, labeler code 52935

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

Yung Zip Chemical Industrial Co., LTD. (labeler code 52935) lists 10 products in the FDA National Drug Code Directory. By type: 10 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on January 19, 2026.

The request: Watch Yung Zip Chemical Industrial Co., LTD. (FDA labeler code 52935): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
52935
Products in commercial distribution
10
Packages
31
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
1
Earliest marketing start
September 4, 1980
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients10100%

Products by type

TypeProductsShare
Bulk ingredients10100%

Dosage forms

Dosage formProductsShare
Powder10100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Edaravone52935-0052PowderBulk ingredientsJanuary 19, 2026
Clonidine hydrochloride52935-0051PowderBulk ingredientsJune 14, 2010
Acyclovir52935-0015PowderBulk ingredientsOctober 20, 2006
Miconazole base52935-0017PowderBulk ingredientsAugust 9, 2006
Econazole nitrate52935-0007PowderBulk ingredientsOctober 14, 1994
Diclofenac potassium52935-0016PowderBulk ingredientsMarch 24, 1994
Miconazole nitrate52935-0009PowderBulk ingredientsMay 27, 1987
Mefenamic acid52935-0008PowderBulk ingredientsDecember 20, 1984
Diclofenac sodium52935-0006PowderBulk ingredientsSeptember 4, 1980
Diclofenac sodium52935-0006PowderBulk ingredientsSeptember 4, 1980

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.