Last Updated: June 6, 2026

Suppliers and packagers for prexxartan


✉ Email this page to a colleague

« Back to Dashboard


prexxartan

Listed suppliers include manufacturers, repackagers, relabelers, and private labeling entitities.

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Carmel Biosciences PREXXARTAN valsartan SOLUTION;ORAL 209139 NDA AptaPharma Inc. 76281-155-56 20 mL in 1 CUP, UNIT-DOSE (76281-155-56) 2026-05-05
Carmel Biosciences PREXXARTAN valsartan SOLUTION;ORAL 209139 NDA AptaPharma Inc. 76281-155-64 120 mL in 1 BOTTLE (76281-155-64) 2026-05-05
Carmel Biosciences PREXXARTAN valsartan SOLUTION;ORAL 209139 NDA AptaPharma Inc. 76281-155-82 473 mL in 1 BOTTLE (76281-155-82) 2026-05-05
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers and packagers for prexxartan

Last updated: May 18, 2026

Suppliers for Prexxartan (Manufacturer, API Sources, and Contract Manufacturing)

Prexxartan suppliers cannot be identified from the information provided. No complete, source-backed list of manufacturers, API vendors, or contract manufacturing organizations can be produced without risking fabrication.

Who supplies Prexxartan drug product and who supplies the API?

No supplier mapping can be produced from the available inputs.

What API suppliers make the active ingredient in Prexxartan?

No API supplier data is available in the provided materials.

Which contract development and manufacturing organizations (CDMOs) can produce Prexxartan?

No CDMO data is available in the provided materials.

Which companies are listed as manufacturers of Prexxartan on FDA labels or approvals?

No FDA label, approval letter, or listing data is provided.

Is Prexxartan sourced from a single manufacturer or multiple parallel sites?

No site- or company-level sourcing data is available in the provided materials.

What is the Orange Book status of Prexxartan and does it indicate supplier identity?

No Orange Book entry, NDC-linked information, or Orange Book patent listing is provided.

How can Orange Book listings reveal drug product manufacturing parties for Prexxartan?

No Orange Book identifiers or listing details are provided.

What generic or biosimilar programs could change Prexxartan supply constraints?

No competitor program information is provided.

Are there Paragraph IV filings tied to Prexxartan that identify manufacturers?

No litigation or filing data is provided.

How does Prexxartan supply depend on key excipients and dosage form manufacturing?

No formulation, dosage form, or CMC package details are provided.

What dosage forms of Prexxartan drive different supplier requirements?

No dosage form or strength information is provided.

What manufacturing and regulatory risks affect Prexxartan supply availability?

No manufacturing site, facility inspection status, or regulatory actions are provided.

Are there known FDA warning letters, import alerts, or 483s tied to Prexxartan suppliers?

No enforcement or inspection record is provided.

Which country sources (API and drug product) typically supply angiotensin receptor blocker assets like Prexxartan?

No country-of-origin sourcing details for Prexxartan are provided.

Are Prexxartan ingredients primarily sourced from India, China, or domestic suppliers?

No sourcing geography is provided.

Key Takeaways

  • A supplier list for Prexxartan (API vendors, drug product manufacturers, or CDMOs) cannot be produced from the information provided.
  • No FDA, Orange Book, label, inspection, or litigation data is available to support supplier identification.
  • No source-backed conclusions on supply chain structure are possible from the current inputs.

FAQs

  1. How can I find the manufacturer of Prexxartan on the FDA label or prescribing information?
  2. Where do Orange Book entries usually list the NDA holder and any listed drug product details?
  3. What sources identify API suppliers when a drug is commercially distributed by a different NDA holder?
  4. How do CDMO manufacturing sites appear in public filings for drug products like Prexxartan?
  5. What public records typically confirm whether a supplier has FDA manufacturing authorization?

References

(No sources were cited because no source-backed supplier or regulatory data for “Prexxartan” was provided.)

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.