Skip to the page

Data / Drug companies / Inventia Healthcare Limited

Inventia Healthcare Limited: 6 products in the FDA NDC directory, labeler code 49252

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

Inventia Healthcare Limited (labeler code 49252) lists 6 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 6 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on May 29, 2020.

The request: Watch Inventia Healthcare Limited (FDA labeler code 49252): 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
49252
Products in commercial distribution
6
Packages
26
Finished drugs by generic name
2
Prescription products
6
Over the counter products
0
Flagged as original packager
6 of 6 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
December 5, 2015
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)6100%

Products by type

TypeProductsShare
Prescription drugs6100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Olmesartan medoxomil331
Duloxetine336

Dosage forms

Dosage formProductsShare
Tablet, coated350%
Capsule, delayed release350%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Olmesartan medoxomil49252-067Tablet, coatedGeneric drugs (ANDA)May 29, 2020
Olmesartan medoxomil49252-066Tablet, coatedGeneric drugs (ANDA)May 29, 2020
Olmesartan medoxomil49252-065Tablet, coatedGeneric drugs (ANDA)May 29, 2020
Duloxetine49252-009Capsule, delayed releaseGeneric drugs (ANDA)December 5, 2015
Duloxetine49252-008Capsule, delayed releaseGeneric drugs (ANDA)December 5, 2015
Duloxetine49252-007Capsule, delayed releaseGeneric drugs (ANDA)December 5, 2015

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.