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Data / Drug companies / Saptalis Pharmaceuticals, LLC.

Saptalis Pharmaceuticals, LLC.: 21 products in the FDA NDC directory, labeler code 71656

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

Saptalis Pharmaceuticals, LLC. (labeler code 71656) lists 21 products in the FDA National Drug Code Directory, covering 18 finished drugs by generic name. By type: 21 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 20, 2026.

The request: Watch Saptalis Pharmaceuticals, LLC. (FDA labeler code 71656): 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
71656
Products in commercial distribution
21
Packages
39
Finished drugs by generic name
18
Prescription products
21
Over the counter products
0
Flagged as original packager
18 of 18 products that carry the flag
Started marketing in the last 12 months
8
Earliest marketing start
September 27, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1990.5%
New drug applications (NDA)14.8%
Authorized generics (NDA)14.8%

Products by type

TypeProductsShare
Prescription drugs21100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Solution1257.1%
Cream314.3%
Concentrate29.5%
Suspension14.8%
Emulsion14.8%
Lotion14.8%
Gel14.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tofacitinib71656-071SolutionGeneric drugs (ANDA)August 20, 2026
Hydroxyzine Hydrochloride71656-090SolutionGeneric drugs (ANDA)June 17, 2026
Fluocinonide71656-094SolutionGeneric drugs (ANDA)May 11, 2026
Desoximetasone71656-087CreamGeneric drugs (ANDA)May 7, 2026
Desoximetasone71656-086CreamGeneric drugs (ANDA)April 13, 2026
Chlorpromazine Hydrochloride71656-102ConcentrateGeneric drugs (ANDA)March 4, 2026
Chlorpromazine Hydrochloride71656-101ConcentrateGeneric drugs (ANDA)March 4, 2026
Cyclosporine71656-012EmulsionGeneric drugs (ANDA)December 12, 2025
Fluoxetine71656-089SolutionGeneric drugs (ANDA)June 20, 2025
Metronidazole vaginal71656-067GelGeneric drugs (ANDA)March 3, 2025
Glycopyrrolate71656-061SolutionGeneric drugs (ANDA)November 25, 2024
Erythromycin topical solution 2%71656-030SolutionGeneric drugs (ANDA)August 14, 2024
Metformin Hydrochloride Oral Solution71656-017SolutionGeneric drugs (ANDA)July 31, 2024
Triamcinolone Acetonide71656-040LotionGeneric drugs (ANDA)July 30, 2024
Lithium71656-072SolutionGeneric drugs (ANDA)March 28, 2024
Hydrocortisone and acetic acid71656-064SolutionAuthorized generics (NDA)February 23, 2024
Levocarnitine71656-016SolutionGeneric drugs (ANDA)February 21, 2024
Likmez71656-066SuspensionNew drug applications (NDA)October 13, 2023
Potassium chloride71656-022SolutionGeneric drugs (ANDA)October 5, 2023
Potassium chloride71656-021SolutionGeneric drugs (ANDA)October 5, 2023
Triamcinolone Acetonide71656-042CreamGeneric drugs (ANDA)September 27, 2023

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.