Skip to the page

Data / Drug companies / Cadila Pharmaceuticals Limited

Cadila Pharmaceuticals Limited: 34 products in the FDA NDC directory, labeler code 65691

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

Cadila Pharmaceuticals Limited (labeler code 65691) 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 May 13, 2026.

The request: Watch Cadila Pharmaceuticals Limited (FDA labeler code 65691): 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
65691
Products in commercial distribution
34
Packages
34
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
2
Earliest marketing start
October 31, 1994
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
Powder3397.1%
Liquid12.9%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Rivaroxaban65691-0128PowderBulk ingredientsMay 13, 2026
Labetalol hydrochloride65691-0091PowderBulk ingredientsMay 12, 2026
Gemfibrozil65691-0089PowderBulk ingredientsJuly 10, 2020
Hydralazine hydrochloride65691-0088PowderBulk ingredientsJuly 3, 2020
Venlafaxine hydrochloride65691-0126PowderBulk ingredientsSeptember 19, 2015
Aripiprazole65691-0052PowderBulk ingredientsSeptember 11, 2015
Bupropion hydrochloride65691-0103PowderBulk ingredientsDecember 31, 2014
Carvedilol65691-0087PowderBulk ingredientsApril 17, 2014
Atorvastatin calcium form-i65691-0090PowderBulk ingredientsApril 15, 2014
Phthaloyl amlodipine65691-0127PowderBulk ingredientsJanuary 30, 2014
Nateglinide form-h65691-0083PowderBulk ingredientsJune 21, 2013
Raloxifene hydrochloride65691-0079PowderBulk ingredientsMay 6, 2013
Bosentan monohydrate65691-0084PowderBulk ingredientsMarch 5, 2013
Valsartan65691-0065PowderBulk ingredientsJuly 7, 2012
Paliperidone65691-0072PowderBulk ingredientsNovember 29, 2010
Olmesartan medoxomil65691-0071PowderBulk ingredientsAugust 26, 2009
Atomoxetine hydrochloride65691-0078PowderBulk ingredientsAugust 11, 2009
Chlorhexidine gluconate solution65691-0051LiquidBulk ingredientsJune 26, 2009
O-desmethyl venlafaxine succinate65691-0067PowderBulk ingredientsJanuary 22, 2009
Escitalopram oxalate65691-0066PowderBulk ingredientsJanuary 6, 2009
Olanzapine form-i65691-0069PowderBulk ingredientsDecember 9, 2008
Sildenafil citrate65691-0063PowderBulk ingredientsDecember 13, 2007
Desloratadine65691-0057PowderBulk ingredientsDecember 11, 2007
Nebivolol hydrochloride65691-0062PowderBulk ingredientsDecember 8, 2007
Alendronate sodium65691-0056PowderBulk ingredientsJuly 11, 2007

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.