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Data / Drug companies / Hikma Pharmaceuticals USA Inc.

Hikma Pharmaceuticals USA Inc.: 10 products in the FDA NDC directory, labeler code 24201

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

Hikma Pharmaceuticals USA Inc. (labeler code 24201) lists 10 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 10 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 1, 2025.

The request: Watch Hikma Pharmaceuticals USA Inc. (FDA labeler code 24201): 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
24201
Products in commercial distribution
10
Packages
13
Finished drugs by generic name
9
Prescription products
10
Over the counter products
0
Controlled substance products
Schedule II 1
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 23, 2019
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)990%
New drug applications (NDA)110%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution770%
Injection, suspension110%
Spray110%
Solution, concentrate110%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Pentobarbital Sodium24201-010Injection, solutionGeneric drugs (ANDA)October 1, 2025
Medroxyprogesterone Acetate Injectable Suspension24201-150Injection, suspensionGeneric drugs (ANDA)May 1, 2023
Acetaminophen24201-110Injection, solutionGeneric drugs (ANDA)March 1, 2023
Acetaminophen24201-100Injection, solutionGeneric drugs (ANDA)March 1, 2023
Levothyroxine Sodium24201-002Injection, solutionNew drug applications (NDA)November 15, 2022
Calcitonin Salmon24201-400Injection, solutionGeneric drugs (ANDA)May 14, 2021
Dihydroergotamine Mesylate24201-463SprayGeneric drugs (ANDA)April 14, 2020
Icatibant24201-207Injection, solutionGeneric drugs (ANDA)March 9, 2020
Sodium Tetradecyl Sulfate24201-201Injection, solutionGeneric drugs (ANDA)December 9, 2019
Valrubicin Intravesical Solution24201-101Solution, concentrateGeneric drugs (ANDA)April 23, 2019

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.