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Data / Drug companies / ScieGen Pharmaceuticals, Inc.

ScieGen Pharmaceuticals, Inc.: 200 products in the FDA NDC directory, labeler code 50228

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

ScieGen Pharmaceuticals, Inc. (labeler code 50228) lists 200 products in the FDA National Drug Code Directory, covering 55 finished drugs by generic name. By type: 198 prescription drugs, 2 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 21, 2026.

The request: Watch ScieGen Pharmaceuticals, Inc. (FDA labeler code 50228): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
50228
Products in commercial distribution
200
Packages
555
Finished drugs by generic name
55
Prescription products
198
Over the counter products
2
Controlled substance products
Schedule IV 1, Schedule V 28
Flagged as original packager
184 of 184 products that carry the flag
Started marketing in the last 12 months
24
Earliest marketing start
January 27, 2014
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)200100%

Products by type

TypeProductsShare
Prescription drugs19899%
Over the counter drugs21%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet7839%
Tablet, film coated5125.5%
Capsule3316.5%
Tablet, film coated, extended release2311.5%
Tablet, extended release84%
Tablet, orally disintegrating42%
Tablet, delayed release21%
Solution10.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Metformin hydrochloride50228-589TabletGeneric drugs (ANDA)August 21, 2026
Metformin hydrochloride50228-588TabletGeneric drugs (ANDA)August 21, 2026
Valsartan and hydrochlorothiazide50228-151Tablet, film coatedGeneric drugs (ANDA)July 27, 2026
Valsartan and hydrochlorothiazide50228-150Tablet, film coatedGeneric drugs (ANDA)July 27, 2026
Valsartan and hydrochlorothiazide50228-149Tablet, film coatedGeneric drugs (ANDA)July 27, 2026
Valsartan and hydrochlorothiazide50228-148Tablet, film coatedGeneric drugs (ANDA)July 27, 2026
Valsartan and hydrochlorothiazide50228-147Tablet, film coatedGeneric drugs (ANDA)July 27, 2026
Tofacitinib citrate50228-567Tablet, film coated, extended releaseGeneric drugs (ANDA)July 14, 2026
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE50228-344Tablet, film coatedGeneric drugs (ANDA)May 19, 2026
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE50228-343Tablet, film coatedGeneric drugs (ANDA)May 19, 2026
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE50228-342Tablet, film coatedGeneric drugs (ANDA)May 19, 2026
Brivaracetam50228-560Tablet, film coatedGeneric drugs (ANDA)March 27, 2026
Brivaracetam50228-559Tablet, film coatedGeneric drugs (ANDA)March 27, 2026
Brivaracetam50228-558Tablet, film coatedGeneric drugs (ANDA)March 27, 2026
Brivaracetam50228-557Tablet, film coatedGeneric drugs (ANDA)March 27, 2026
Brivaracetam50228-556Tablet, film coatedGeneric drugs (ANDA)March 27, 2026
Pregabalin50228-652CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-651CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-650CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-649CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-648CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-647CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-646CapsuleGeneric drugs (ANDA)December 10, 2025
Pregabalin50228-645CapsuleGeneric drugs (ANDA)December 10, 2025
Ticagrelor50228-522TabletGeneric drugs (ANDA)October 9, 2025

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.