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Data / Drug companies / Xellia Pharmaceuticals USA LLC

Xellia Pharmaceuticals USA LLC: 36 products in the FDA NDC directory, labeler code 70594

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

Xellia Pharmaceuticals USA LLC (labeler code 70594) lists 36 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 36 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on November 3, 2023.

The request: Watch Xellia Pharmaceuticals USA LLC (FDA labeler code 70594): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
70594
Products in commercial distribution
36
Packages
42
Finished drugs by generic name
13
Prescription products
36
Over the counter products
0
Flagged as original packager
36 of 36 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
February 23, 2016
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)2569.4%
New drug applications (NDA)1130.6%

Products by type

TypeProductsShare
Prescription drugs36100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution1644.4%
Injection, powder, lyophilized, for solution822.2%
Injection616.7%
Injection, powder, for solution513.9%
Solution12.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Daptomycin70594-066Injection, powder, lyophilized, for solutionNew drug applications (NDA)November 3, 2023
Daptomycin70594-060Injection, powder, lyophilized, for solutionNew drug applications (NDA)November 3, 2023
Carboprost Tromethamine70594-112SolutionGeneric drugs (ANDA)November 1, 2023
Voriconazole70594-067Injection, powder, lyophilized, for solutionNew drug applications (NDA)August 24, 2023
Bupivacaine HCl70594-119Injection, solutionGeneric drugs (ANDA)August 1, 2023
Bupivacaine HCl70594-116Injection, solutionGeneric drugs (ANDA)August 1, 2023
Acetylcysteine70594-111Injection, solutionGeneric drugs (ANDA)June 10, 2023
Bupivacine HCl70594-121Injection, solutionGeneric drugs (ANDA)June 1, 2023
Bupivacaine HCl70594-120Injection, solutionGeneric drugs (ANDA)June 1, 2023
Bupivacaine HCl70594-118Injection, solutionGeneric drugs (ANDA)June 1, 2023
Bupivacaine HCl70594-117Injection, solutionGeneric drugs (ANDA)June 1, 2023
BUPIVACAINE HCl70594-115Injection, solutionGeneric drugs (ANDA)June 1, 2023
Bupivacaine HCl70594-114Injection, solutionGeneric drugs (ANDA)June 1, 2023
Colistimethate70594-023Injection, powder, for solutionGeneric drugs (ANDA)February 20, 2022
Sumatriptan70594-068InjectionGeneric drugs (ANDA)January 1, 2022
Phenylephrine Hydrochloride70594-065InjectionGeneric drugs (ANDA)January 1, 2022
Phenylephrine Hydrochloride70594-064InjectionGeneric drugs (ANDA)January 1, 2022
Phenylephrine Hydrochloride70594-063InjectionGeneric drugs (ANDA)January 1, 2022
Meropenem70594-076Injection, powder, for solutionGeneric drugs (ANDA)June 28, 2021
Meropenem70594-075Injection, powder, for solutionGeneric drugs (ANDA)June 28, 2021
Daptomycin70594-034Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 1, 2021
Neostigmine Methylsulfate70594-072InjectionGeneric drugs (ANDA)January 10, 2021
Neostigmine Methylsulfate70594-069InjectionGeneric drugs (ANDA)January 10, 2021
Vancomycin70594-058Injection, solutionNew drug applications (NDA)May 13, 2020
Vancomycin70594-056Injection, solutionNew drug applications (NDA)May 13, 2020

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.