Last Updated: August 8, 2026

Suppliers and packagers for NULIBRY


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NULIBRY

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Sentynl Theraps Inc NULIBRY fosdenopterin hydrobromide POWDER;INTRAVENOUS 214018 NDA Sentynl Therapeutics, Inc. 42358-295-01 1 VIAL, SINGLE-DOSE in 1 CARTON (42358-295-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE 2021-03-30
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers and packagers for NULIBRY

Last updated: June 7, 2026

Nulibry (Nalmefene?) Suppliers: Who Makes the Drug Product, API, and Key Components?

No complete, accurate supplier roster for Nulibry (including drug product manufacturer, API source(s), contract manufacturing organizations, or raw-material suppliers) can be produced from the information provided in the prompt alone.

Which companies supply Nulibry drug product and finished dosage form?

No verifiable, source-backed manufacturer list is available from the prompt.

Are there multiple CMO sites manufacturing Nulibry tablets/capsules/injection?

No verifiable CMO site list is available from the prompt.

Which labeler is shown on Nulibry packaging?

No packaging-labeler evidence is available from the prompt.

Who supplies the active pharmaceutical ingredient (API) for Nulibry?

No verifiable API supplier(s) can be produced from the prompt.

What API manufacturing plants are used for Nulibry?

No plant-level evidence is available from the prompt.

Is Nulibry’s API sourced from contract suppliers or internal manufacturing?

No sourcing model evidence is available from the prompt.

What patents or exclusivity constrain Nulibry’s supply chain?

No Orange Book, patent, or exclusivity mapping is available from the prompt.

How does exclusivity affect supplier onboarding for generics or biosimilars of Nulibry?

No regulatory exclusivity status is available from the prompt.

What regulatory filings identify Nulibry suppliers (FDA, NDA/ANDA, DMF)?

No FDA filing trail (NDA/ANDA number, DMF references, or listed manufacturers) is available from the prompt.

Which DMFs are linked to Nulibry’s API and intermediates?

No DMF-linked evidence is available from the prompt.

How do Nulibry supply constraints impact price, shortages, and launch timing?

No manufacturer and sourcing data is available from the prompt.

What generic entry risks exist if supplier capacity is limited for Nulibry?

No supplier-capacity or product/route-of-synthesis data is available from the prompt.

Which contract manufacturing and packaging vendors support Nulibry?

No CMO/CSP/packaging vendor list is available from the prompt.

Key Takeaways

  • A complete, accurate supplier map for Nulibry cannot be generated from the prompt alone.
  • No evidence is available here for drug product manufacturers, API suppliers, CMO sites, or DMF-linked sourcing.

FAQs

  1. How can I identify the labeler and manufacturer for Nulibry from FDA or commercial listings?
  2. Does Nulibry use a single API supplier or multiple qualified sources?
  3. Which DMFs typically cover API intermediates for small-molecule drugs like Nulibry?
  4. How do CMO and packaging suppliers influence Nulibry availability during demand spikes?
  5. What documentation most directly connects Nulibry manufacturing sites to regulatory filings?

References

No sources were cited because no supplier, regulatory, or patent information was provided in the prompt.

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