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Data / Drug companies / Medilux Laboratories Private Limited

Medilux Laboratories Private Limited: 9 products in the FDA NDC directory, labeler code 50218

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

Medilux Laboratories Private Limited (labeler code 50218) 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 April 25, 2025.

The request: Watch Medilux Laboratories Private Limited (FDA labeler code 50218): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
50218
Products in commercial distribution
9
Packages
25
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
July 1, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients666.7%
Bulk ingredients for compounding333.3%

Products by type

TypeProductsShare
Bulk ingredients9100%

Dosage forms

Dosage formProductsShare
Powder9100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Bumetanide50218-017PowderBulk ingredientsApril 25, 2025
Trazodone hydrochloride50218-016PowderBulk ingredientsOctober 1, 2024
Baclofen50218-015PowderBulk ingredientsOctober 1, 2024
Torsemide50218-014PowderBulk ingredientsMay 21, 2024
Buspirone hydrochloride50218-013PowderBulk ingredients for compoundingApril 17, 2024
Bromfenac sodium hydrate50218-012PowderBulk ingredients for compoundingApril 11, 2024
Dapsone50218-008PowderBulk ingredientsMarch 19, 2019
Baclofen50218-010PowderBulk ingredients for compoundingNovember 15, 2016
Hydroquinone50218-009PowderBulk ingredientsJuly 1, 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.