Skip to the page

Data / Drug companies / Valary Lab Private Limited

Valary Lab Private Limited: 32 products in the FDA NDC directory, labeler code 81955

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

Valary Lab Private Limited (labeler code 81955) lists 32 products in the FDA National Drug Code Directory. By type: 32 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on April 26, 2023.

The request: Watch Valary Lab Private Limited (FDA labeler code 81955): 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
81955
Products in commercial distribution
32
Packages
36
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 17, 1964
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients32100%

Products by type

TypeProductsShare
Bulk ingredients32100%

Dosage forms

Dosage formProductsShare
Powder32100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Niraparib tosylate monohydrate81955-0016PowderBulk ingredientsApril 26, 2023
Dabrafenib mesylate81955-0029PowderBulk ingredientsMarch 16, 2023
Lenalidomide hemihydrate (form-b)81955-0013PowderBulk ingredientsOctober 14, 2021
Belzutifan81955-0025PowderBulk ingredientsAugust 13, 2021
Tivozanib hydrochloride monohydrate81955-0023PowderBulk ingredientsMarch 10, 2021
Pralsetinib81955-0018PowderBulk ingredientsSeptember 4, 2020
Azacitidine81955-0012PowderBulk ingredientsSeptember 1, 2020
Tucatinib hemiethanolate81955-0033PowderBulk ingredientsApril 17, 2020
Selumetinib sulfate premix81955-0031PowderBulk ingredientsApril 10, 2020
Selumetinib sulfate81955-0030PowderBulk ingredientsApril 10, 2020
Encorafenib81955-0026PowderBulk ingredientsJune 27, 2018
Binimetinib81955-0022PowderBulk ingredientsJune 27, 2018
Ribociclib succinate81955-0003PowderBulk ingredientsMarch 13, 2017
Ethinyl estradiol81955-0024PowderBulk ingredientsAugust 12, 2015
Trametinib dimethyl sulfoxide81955-0020PowderBulk ingredientsMay 29, 2013
Cabozantinib malate81955-0021PowderBulk ingredientsNovember 29, 2012
Ruxolitinib phosphate81955-0019PowderBulk ingredientsNovember 16, 2011
Gemcitabine81955-0006PowderBulk ingredientsJuly 25, 2011
Temozolomide81955-0014PowderBulk ingredientsMarch 1, 2010
Bendamustine hydrochloride81955-0011PowderBulk ingredientsMarch 20, 2008
Nilotinib hydrochloride81955-0017PowderBulk ingredientsOctober 29, 2007
Lenalidomide (form-h1)81955-0008PowderBulk ingredientsJune 29, 2006
Erlotinib hydrochloride81955-0010PowderBulk ingredientsNovember 8, 2004
Levonorgestrel81955-0027PowderBulk ingredientsNovember 21, 2003
Imatinib mesylate81955-0002PowderBulk ingredientsApril 18, 2003

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.