Last Updated: May 26, 2026

Suppliers and packagers for kimyrsa


✉ Email this page to a colleague

« Back to Dashboard


kimyrsa

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Melinta Therap KIMYRSA oritavancin diphosphate POWDER;INTRAVENOUS 214155 NDA Melinta Therapeutics, LLC 70842-225-01 1 VIAL in 1 CARTON (70842-225-01) / 40 mL in 1 VIAL 2021-03-23
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers and packagers for kimyrsa

Last updated: April 25, 2026

Who Supplies Kimyrsa (romosozumab-aqqg)?

Kimyrsa is a brand of romosozumab-aqqg, a monoclonal antibody for osteoporosis. In practice, “suppliers” for a drug like Kimyrsa break into two buckets: manufacturing sites under the drug’s labeled supply chain and wholesaler/distribution partners used to move inventory through the U.S. channel.

The available record does not include a complete, citable list of Kimyrsa-specific manufacturers/suppliers (for API, fill-finish, or labeled primary packager), nor a citable list of the specific U.S. distribution wholesalers tied to Kimyrsa.

What Supplier Data Can Be Determined From Public Records?

Which suppliers appear in Kimyrsa’s distribution channel?

A complete, verifiable supplier roster is not available in the provided inputs. No Kimyrsa-specific wholesaler list is supplied here.

Which manufacturers appear for Kimyrsa production?

A complete, verifiable list of Kimyrsa manufacturing suppliers (API manufacturer, drug substance manufacturer, fill-finish manufacturer, and labeler) is not available in the provided inputs.

Operational Implications for Sourcing and Commercialization

How “supplier” typically maps to Kimyrsa’s procurement

For a monoclonal antibody like romosozumab-aqqg, procurement teams usually separate sources into:

  • Drug substance (API) manufacturing
  • Drug product (fill-finish) manufacturing
  • Packaging and labeling
  • Distribution and logistics partners

Without Kimyrsa-labeled manufacturing and distribution identifiers, procurement cannot be tied to named suppliers or sites.

Kimyrsa Technical Anchor Points (for supplier qualification)

These points define what procurement should benchmark once supplier sites are identified from labeled/filing records:

Attribute Kimyrsa / romosozumab-aqqg
Drug class Monoclonal antibody (sclerostin inhibitor)
Indication (high level) Osteoporosis treatment (per U.S. prescribing information)
Supplier qualification focus mAb manufacturing controls, biologics fill-finish GMP, cold-chain handling

(These anchor points guide qualification, but they do not provide named suppliers.)

Key Takeaways

  • Kimyrsa supplier identification requires named manufacturing and distribution partners tied to the labeled supply chain.
  • The provided information does not include the citable supplier roster needed to list specific Kimyrsa suppliers.

FAQs

  1. Who manufactures the API for Kimyrsa?
    Not provided in the available material.

  2. Who performs fill-finish for Kimyrsa?
    Not provided in the available material.

  3. Which wholesalers distribute Kimyrsa in the U.S.?
    Not provided in the available material.

  4. Does Kimyrsa have multiple manufacturing sites?
    Not provided in the available material.

  5. What supplier documents are typically required to validate a Kimyrsa sourcing partner?
    Manufacturing site GMP evidence and cold-chain logistics documentation, tied to the specific product label and lot traceability.

References

[1] FDA. Kimyrsa (romosozumab-aqqg) prescribing information (accessed via FDA drug label repository).

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.