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Data / Drug companies / Mylan Pharmaceuticals Inc.

Mylan Pharmaceuticals Inc.: 78 products in the FDA NDC directory, labeler code 59762

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

Mylan Pharmaceuticals Inc. (labeler code 59762) lists 78 products in the FDA National Drug Code Directory, covering 36 finished drugs by generic name. By type: 78 prescription drugs. Its main marketing category is authorized generics (NDA). The newest product started marketing on August 3, 2026.

The request: Watch Mylan Pharmaceuticals Inc. (FDA labeler code 59762): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
59762
Products in commercial distribution
78
Packages
110
Finished drugs by generic name
36
Prescription products
78
Over the counter products
0
Controlled substance products
Schedule IV 10, Schedule V 2
Flagged as original packager
75 of 75 products that carry the flag
Started marketing in the last 12 months
1
Products with a marketing end date set
4
Earliest marketing start
June 3, 1959
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Authorized generics (NDA)7798.7%
Generic drugs (ANDA)11.3%

Products by type

TypeProductsShare
Prescription drugs78100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet3950%
Tablet, film coated1012.8%
Tablet, extended release45.1%
Tablet, sugar coated45.1%
Solution45.1%
Powder, for suspension33.8%
Suspension33.8%
Capsule, gelatin coated22.6%
Tablet, delayed release22.6%
Cream22.6%
Granule, for suspension11.3%
Lotion11.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Doxazosin mesylate59762-1391TabletAuthorized generics (NDA)August 3, 2026
Doxazosin mesylate59762-1390TabletAuthorized generics (NDA)September 24, 2025
Doxazosin mesylate59762-1389TabletAuthorized generics (NDA)May 9, 2025
Doxazosin mesylate59762-1388TabletAuthorized generics (NDA)May 9, 2025
Eplerenone59762-1107Tablet, film coatedAuthorized generics (NDA)December 13, 2024
Eplerenone59762-1108Tablet, film coatedAuthorized generics (NDA)November 14, 2024
Doxazosin59762-2440TabletAuthorized generics (NDA)January 18, 2023
Gabapentin59762-5050SuspensionAuthorized generics (NDA)July 1, 2022
Doxazosin59762-2480TabletAuthorized generics (NDA)October 19, 2021
Doxazosin59762-2420TabletAuthorized generics (NDA)October 19, 2021
Phenytoin59762-0531SuspensionAuthorized generics (NDA)April 22, 2020
Ethosuximide59762-2350SolutionGeneric drugs (ANDA)February 21, 2020
Pregabalin59762-1576SolutionAuthorized generics (NDA)July 29, 2019
Sirolimus59762-1205SolutionAuthorized generics (NDA)July 22, 2019
Amlodipine besylate59762-2242TabletAuthorized generics (NDA)June 24, 2019
Amlodipine besylate59762-2135TabletAuthorized generics (NDA)June 24, 2019
Amlodipine besylate59762-2010TabletAuthorized generics (NDA)June 24, 2019
Liothyronine Sodium59762-1208TabletAuthorized generics (NDA)June 24, 2019
Liothyronine Sodium59762-1207TabletAuthorized generics (NDA)June 24, 2019
Disopyramide Phosphate59762-0400Capsule, gelatin coatedAuthorized generics (NDA)April 23, 2019
Disopyramide Phosphate59762-0386Capsule, gelatin coatedAuthorized generics (NDA)April 23, 2019
Liothyronine Sodium59762-1206TabletAuthorized generics (NDA)February 6, 2019
Medroxyprogesterone acetate59762-0058TabletAuthorized generics (NDA)August 20, 2018
Medroxyprogesterone acetate59762-0055TabletAuthorized generics (NDA)August 19, 2018
Sertraline hydrochloride59762-0067Solution, concentrateAuthorized generics (NDA)May 15, 2018

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.