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Data / Drug companies / Amerisyn LLC

Amerisyn LLC: 26 products in the FDA NDC directory, labeler code 87564

Amerisyn LLC (labeler code 87564) lists 26 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 26 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 7, 2026.

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
87564
Products in commercial distribution
26
Packages
36
Finished drugs by generic name
9
Prescription products
26
Over the counter products
0
Flagged as original packager
22 of 22 products that carry the flag
Started marketing in the last 12 months
26
Earliest marketing start
June 30, 2026
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)26100%

Products by type

TypeProductsShare
Prescription drugs26100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule1350%
Tablet, film coated519.2%
Tablet, orally disintegrating519.2%
Tablet311.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Terazosin hydrochloride87564-084CapsuleGeneric drugs (ANDA)August 7, 2026
Terazosin hydrochloride87564-083CapsuleGeneric drugs (ANDA)August 7, 2026
Terazosin hydrochloride87564-082CapsuleGeneric drugs (ANDA)August 7, 2026
Terazosin hydrochloride87564-081CapsuleGeneric drugs (ANDA)August 7, 2026
Mexiletine hydrochloride87564-054CapsuleGeneric drugs (ANDA)August 6, 2026
Mexiletine hydrochloride87564-053CapsuleGeneric drugs (ANDA)August 6, 2026
Mexiletine hydrochloride87564-052CapsuleGeneric drugs (ANDA)August 6, 2026
Ketoconazole87564-051TabletGeneric drugs (ANDA)August 6, 2026
Risperidone87564-017Tablet, orally disintegratingGeneric drugs (ANDA)August 6, 2026
Risperidone87564-016Tablet, orally disintegratingGeneric drugs (ANDA)August 6, 2026
Risperidone87564-015Tablet, orally disintegratingGeneric drugs (ANDA)August 6, 2026
Risperidone87564-014Tablet, orally disintegratingGeneric drugs (ANDA)August 6, 2026
Risperidone87564-013Tablet, orally disintegratingGeneric drugs (ANDA)August 6, 2026
Terbinafine87564-010TabletGeneric drugs (ANDA)August 3, 2026
Nicardipine hydrochloride87564-028CapsuleGeneric drugs (ANDA)July 26, 2026
Nicardipine hydrochloride87564-027CapsuleGeneric drugs (ANDA)July 26, 2026
Ketorolac Tromethamine87564-018Tablet, film coatedGeneric drugs (ANDA)July 26, 2026
Diclofenac potassium87564-011TabletGeneric drugs (ANDA)July 26, 2026
Terazosin Hydrochloride87564-009CapsuleGeneric drugs (ANDA)July 1, 2026
Terazosin Hydrochloride87564-008CapsuleGeneric drugs (ANDA)July 1, 2026
Terazosin Hydrochloride87564-007CapsuleGeneric drugs (ANDA)July 1, 2026
Terazosin Hydrochloride87564-006CapsuleGeneric drugs (ANDA)July 1, 2026
Eltrombopag olamine87564-035Tablet, film coatedGeneric drugs (ANDA)June 30, 2026
Eltrombopag olamine87564-034Tablet, film coatedGeneric drugs (ANDA)June 30, 2026
Eltrombopag olamine87564-033Tablet, film coatedGeneric drugs (ANDA)June 30, 2026

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