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Data / Drug companies / Hubei Honch Pharmaceutical Co., Ltd.

Hubei Honch Pharmaceutical Co., Ltd.: 12 products in the FDA NDC directory, labeler code 62158

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

Hubei Honch Pharmaceutical Co., Ltd. (labeler code 62158) lists 12 products in the FDA National Drug Code Directory. By type: 12 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on October 1, 2025.

The request: Watch Hubei Honch Pharmaceutical Co., Ltd. (FDA labeler code 62158): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
62158
Products in commercial distribution
12
Packages
13
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
February 28, 2014
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients12100%

Products by type

TypeProductsShare
Bulk ingredients12100%

Dosage forms

Dosage formProductsShare
Powder12100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Bleomycin sulfate62158-0013PowderBulk ingredientsOctober 1, 2025
Vinblastine sulfate62158-0012PowderBulk ingredientsOctober 1, 2025
Bortezomib62158-0011PowderBulk ingredientsDecember 1, 2021
Vincristine sulfate62158-0010PowderBulk ingredientsDecember 1, 2021
Spinosad62158-0009PowderBulk ingredientsSeptember 23, 2021
Ixabepilone62158-0008PowderBulk ingredientsJune 30, 2021
Melphalan hcl62158-0007PowderBulk ingredientsFebruary 8, 2021
Nitenpyram62158-0006PowderBulk ingredientsFebruary 8, 2021
Mitomycin62158-0005PowderBulk ingredientsAugust 1, 2019
Lufenuron62158-0004PowderBulk ingredientsNovember 20, 2018
Milbemycin oxime62158-0003PowderBulk ingredientsOctober 27, 2014
Vinorelbine tartrate62158-0001PowderBulk ingredientsFebruary 28, 2014

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.