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

Hubei JXBio Pharmaceutical Co.,Ltd: 9 products in the FDA NDC directory, labeler code 76617

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

Hubei JXBio Pharmaceutical Co.,Ltd (labeler code 76617) lists 9 products in the FDA National Drug Code Directory. By type: 9 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on October 26, 2026.

The request: Watch Hubei JXBio Pharmaceutical Co.,Ltd (FDA labeler code 76617): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
76617
Products in commercial distribution
9
Packages
37
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
4
Earliest marketing start
April 24, 2020
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients555.6%
Bulk ingredients for compounding444.4%

Products by type

TypeProductsShare
Bulk ingredients9100%

Dosage forms

Dosage formProductsShare
Powder9100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Atosiban acetate76617-008PowderBulk ingredientsOctober 26, 2026
Octreotide acetate76617-007PowderBulk ingredientsOctober 15, 2026
Leuprorelin acetate76617-006PowderBulk ingredientsJanuary 1, 2026
Sermorelin acetate76617-005PowderBulk ingredients for compoundingDecember 16, 2025
Semaglutide76617-003PowderBulk ingredientsJanuary 9, 2025
Liraglutide76617-002PowderBulk ingredients for compoundingMarch 14, 2024
Tirzepatide76617-020PowderBulk ingredients for compoundingDecember 5, 2022
Semaglutide76617-001PowderBulk ingredients for compoundingNovember 17, 2022
Oxytocin76617-011PowderBulk ingredientsApril 24, 2020

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.