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Data / Drug companies / Aarti Pharmalabs Limited

Aarti Pharmalabs Limited: 34 products in the FDA NDC directory, labeler code 15308

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

Aarti Pharmalabs Limited (labeler code 15308) lists 34 products in the FDA National Drug Code Directory. By type: 34 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on March 3, 2025.

The request: Watch Aarti Pharmalabs Limited (FDA labeler code 15308): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
15308
Products in commercial distribution
34
Packages
35
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
January 1, 1983
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients34100%

Products by type

TypeProductsShare
Bulk ingredients34100%

Dosage forms

Dosage formProductsShare
Powder34100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Enalapril maleate15308-2601PowderBulk ingredientsMarch 3, 2025
Ibrutinib15308-2402PowderBulk ingredientsJanuary 31, 2024
Palbociclib15308-2401PowderBulk ingredientsJanuary 31, 2024
Deferiprone15308-2908PowderBulk ingredientsApril 16, 2023
Cyclophosphamide15308-0921PowderBulk ingredientsSeptember 27, 2021
Apixaban15308-1221PowderBulk ingredientsJuly 1, 2021
Enzalutamide15308-1121PowderBulk ingredientsApril 28, 2021
Fluticasone furoate15308-2021PowderBulk ingredientsJuly 14, 2020
Ramipril15308-0300PowderBulk ingredientsAugust 30, 2016
Salmeterol xinafoate15308-1021PowderBulk ingredientsJanuary 21, 2016
Venlafaxine hydrochloride polymorph b15308-1506PowderBulk ingredientsDecember 14, 2012
Diflunisal15308-0811PowderBulk ingredientsApril 8, 2012
Loteprednol etabonate15308-0722PowderBulk ingredientsJune 30, 2011
Bupropion hydrochloride15308-0412PowderBulk ingredientsMarch 24, 2010
Bicalutamide15308-0360PowderBulk ingredientsAugust 1, 2009
Ranolazine15308-0718PowderBulk ingredientsJanuary 1, 2008
Mometasone furoate monohydrate15308-2710PowderBulk ingredientsJanuary 1, 2006
Mometasone furoate15308-0220PowderBulk ingredientsJanuary 1, 2006
Fluticasone propionate15308-0200PowderBulk ingredientsJanuary 1, 2005
Azathioprine15308-0732PowderBulk ingredientsFebruary 3, 2004
Ipratropium bromide15308-1001PowderBulk ingredientsJanuary 1, 2002
Mesna15308-0715PowderBulk ingredientsJanuary 1, 2002
Budesonide15308-0100PowderBulk ingredientsJanuary 1, 2001
Levalbuterol hydrochloride15308-0310PowderBulk ingredientsJanuary 1, 2000
Capecitabine15308-0714PowderBulk ingredientsJanuary 1, 1999

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.