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Data / Drug companies / Veranova, L.P.

Veranova, L.P.: 45 products in the FDA NDC directory, labeler code 49812

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

Veranova, L.P. (labeler code 49812) lists 45 products in the FDA National Drug Code Directory. By type: 45 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on January 8, 2026.

The request: Watch Veranova, L.P. (FDA labeler code 49812): 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
49812
Products in commercial distribution
45
Packages
46
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 28, Schedule III 2
Started marketing in the last 12 months
1
Earliest marketing start
January 1, 1985
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients45100%

Products by type

TypeProductsShare
Bulk ingredients45100%

Dosage forms

Dosage formProductsShare
Powder4497.8%
Oil12.2%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lisdexamfetamine dimesylate49812-0307PowderBulk ingredientsJanuary 8, 2026
Hydromorphone hcl49812-0306PowderBulk ingredientsApril 15, 2025
Racemic amphetamine aspartate49812-0295PowderBulk ingredientsSeptember 1, 2021
Dexmethylphenidate hcl49812-0076PowderBulk ingredientsSeptember 12, 2019
Codeine phosphate hemihydrate49812-0051PowderBulk ingredientsSeptember 6, 2019
Phytonadione49812-0232PowderBulk ingredientsJanuary 1, 2016
Diphenoxylate hcl49812-0248PowderBulk ingredientsJanuary 14, 2014
Carboplatin49812-0010PowderBulk ingredientsJanuary 14, 2014
Lurasidone hcl49812-0270PowderBulk ingredientsJanuary 1, 2014
Dofetilide49812-0261PowderBulk ingredientsJanuary 1, 2014
Hydrocodone bitartrate enol benzoate hcl49812-0220PowderBulk ingredientsJanuary 1, 2014
Oxymorphone hcl49812-0136PowderBulk ingredientsJune 1, 2012
Dimethyl fumarate49812-0255PowderBulk ingredientsJanuary 1, 2012
Naloxone hcl49812-0195PowderBulk ingredientsJanuary 1, 2012
Remifentanil hcl49812-0190PowderBulk ingredientsJanuary 1, 2012
Lisdexfetamine dimesylate49812-0186PowderBulk ingredientsJanuary 1, 2012
Nabilone49812-0156PowderBulk ingredientsJanuary 1, 2012
Sodium oxybate49812-0207PowderBulk ingredientsJune 1, 2010
Methylphenidate base49812-0163PowderBulk ingredientsJune 1, 2010
Oxycodone hcl49812-0150PowderBulk ingredientsJune 1, 2010
Methylphenidate hcl49812-0020PowderBulk ingredientsJune 1, 2010
Methamphetamine hcl49812-0183PowderBulk ingredientsJanuary 1, 2009
6 % tetrahydrocannabinol in sesame oil49812-0113OilBulk ingredientsJanuary 1, 2008
Sufentanil base49812-0110PowderBulk ingredientsJune 9, 2005
Morphine sulfate49812-0149PowderBulk ingredientsJanuary 1, 2005

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.