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Data / Drug companies / Umedica Laboratories USA Inc.

Umedica Laboratories USA Inc.: 52 products in the FDA NDC directory, labeler code 60290

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

Umedica Laboratories USA Inc. (labeler code 60290) lists 52 products in the FDA National Drug Code Directory, covering 18 finished drugs by generic name. By type: 52 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 10, 2026.

The request: Watch Umedica Laboratories USA Inc. (FDA labeler code 60290): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
60290
Products in commercial distribution
52
Packages
164
Finished drugs by generic name
18
Prescription products
52
Over the counter products
0
Controlled substance products
Schedule IV 1
Flagged as original packager
3 of 3 products that carry the flag
Started marketing in the last 12 months
45
Earliest marketing start
April 21, 2020
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)52100%

Products by type

TypeProductsShare
Prescription drugs52100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet2038.5%
Tablet, film coated1528.8%
Capsule713.5%
Tablet, extended release59.6%
Tablet, delayed release35.8%
Powder, for solution11.9%
Kit11.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sacubitril and Valsartan60290-087Tablet, film coatedGeneric drugs (ANDA)August 10, 2026
Sacubitril and Valsartan60290-086Tablet, film coatedGeneric drugs (ANDA)August 10, 2026
Sacubitril and Valsartan60290-085Tablet, film coatedGeneric drugs (ANDA)August 10, 2026
Ranolazine60290-056Tablet, extended releaseGeneric drugs (ANDA)August 10, 2026
Ranolazine60290-055Tablet, extended releaseGeneric drugs (ANDA)August 10, 2026
Zolpidem Tartrate60290-089CapsuleGeneric drugs (ANDA)May 14, 2026
Olmesartan Medoxomil and Hydrochlorothiazide60290-102TabletGeneric drugs (ANDA)February 15, 2026
Diclofenac Sodium60290-084Tablet, delayed releaseGeneric drugs (ANDA)February 15, 2026
Diclofenac Sodium60290-083Tablet, delayed releaseGeneric drugs (ANDA)February 15, 2026
Diclofenac Sodium60290-082Tablet, delayed releaseGeneric drugs (ANDA)February 15, 2026
Sildenafil citrate60290-079Tablet, film coatedGeneric drugs (ANDA)February 15, 2026
Sertraline HCl60290-071CapsuleGeneric drugs (ANDA)February 15, 2026
Sertraline HCl60290-070CapsuleGeneric drugs (ANDA)February 15, 2026
Diclofenac potassium60290-061Powder, for solutionGeneric drugs (ANDA)February 15, 2026
Atorvastatin calcium60290-042TabletGeneric drugs (ANDA)February 15, 2026
Atorvastatin calcium60290-041TabletGeneric drugs (ANDA)February 15, 2026
Atorvastatin calcium60290-040TabletGeneric drugs (ANDA)February 15, 2026
Atorvastatin calcium60290-039TabletGeneric drugs (ANDA)February 15, 2026
Tadalafil60290-030Tablet, film coatedGeneric drugs (ANDA)February 15, 2026
Tadalafil60290-029Tablet, film coatedGeneric drugs (ANDA)February 15, 2026
Tadalafil60290-028Tablet, film coatedGeneric drugs (ANDA)February 15, 2026
Tadalafil60290-027Tablet, film coatedGeneric drugs (ANDA)February 15, 2026
Olmesartan Medoxomil and Hydrochlorothiazide60290-026TabletGeneric drugs (ANDA)February 15, 2026
Olmesartan Medoxomil and Hydrochlorothiazide60290-025TabletGeneric drugs (ANDA)February 15, 2026
Celecoxib60290-019CapsuleGeneric drugs (ANDA)February 15, 2026

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.