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Data / Drug companies / Horster Biotek PVT LTD.

Horster Biotek PVT LTD.: 6 products in the FDA NDC directory, labeler code 85568

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

Horster Biotek PVT LTD. (labeler code 85568) lists 6 products in the FDA National Drug Code Directory. By type: 6 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on April 24, 2025.

The request: Watch Horster Biotek PVT LTD. (FDA labeler code 85568): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
85568
Products in commercial distribution
6
Packages
39
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule III 3
Started marketing in the last 12 months
0
Earliest marketing start
April 22, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients350%
Bulk ingredients for compounding350%

Products by type

TypeProductsShare
Bulk ingredients6100%

Dosage forms

Dosage formProductsShare
Powder6100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tadalafil85568-006PowderBulk ingredientsApril 24, 2025
Methylcobalamin85568-005PowderBulk ingredientsApril 24, 2025
Progesterone85568-004PowderBulk ingredients for compoundingApril 23, 2025
Stanozolol85568-003PowderBulk ingredients for compoundingApril 23, 2025
Oxymetholone85568-002PowderBulk ingredientsApril 22, 2025
Oxandrolone85568-001PowderBulk ingredients for compoundingApril 22, 2025

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.