Last Updated: June 25, 2026

Suppliers and packagers for brynovin


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brynovin

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Azurity BRYNOVIN sitagliptin hydrochloride SOLUTION;ORAL 219122 NDA Azurity Pharmaceuticals, Inc. 24338-017-01 1 BOTTLE in 1 CARTON (24338-017-01) / 120 mL in 1 BOTTLE 2025-04-01
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Last updated: June 7, 2026

ecutive summary: No complete, verifiable drug-identity inputs are provided for “BRYNOVIN” (active ingredient, dosage form/strength, country/brand owner, or FDA/NDC label). Without that, it is not possible to produce an accurate supplier map (API/manufacturer, contract manufacturing, packaging, or distributor network) suitable for patent, regulatory, or commercial use.

Suppliers for BRYNOVIN (drug brand)

Answer: Not available from the provided input. A supplier list requires the underlying drug identity (INN, dosage form/strength, and jurisdiction) to link to label, NDC/GTIN, Orange Book/Drug List entries, and cGMP manufacturing sites.

What counts as a “supplier” for BRYNOVIN?

  • API supplier (active pharmaceutical ingredient manufacturer, including DMF holders if applicable)
  • Finished dosage manufacturer (tablet/capsule/sterile fill-finish site)
  • Packager/labeler (secondary packaging and labeling)
  • Market distributor (wholesaler and channel partners tied to the labeled NDC)

What company manufactures BRYNOVIN?

Answer: Not available from the provided input.

Which manufacturing sites typically appear on the BRYNOVIN label?

  • The labeled manufacturer and packager/labeler listed on the product label and NDC record.
  • For sterile products, the fill-finish site is often separate from API production.

Who supplies the API for BRYNOVIN?

Answer: Not available from the provided input.

How to identify the API manufacturer in practice

  • Link brand to its INN and strength/dosage form, then use:
    • FDA Drugs@FDA label (for U.S.)
    • Orange Book (if applicable)
    • DMF references when disclosed
    • Third-party cGMP databases only after product identity is confirmed

What are BRYNOVIN’s contract manufacturing partners (CMOs)?

Answer: Not available from the provided input.

Common CMO roles

  • Solid oral CMOs (blending, granulation, tableting, coating, blistering/bottling)
  • Sterile CMOs (if applicable): aseptic fill-finish, lyophilization, sterilization

What is the Orange Book status of BRYNOVIN (and does it affect suppliers)?

Answer: Not available from the provided input.

How Orange Book data drives supplier mapping

  • Orange Book listings can connect to:
    • Approved application holder
    • Patent-protected components (which can narrow possible API/finish suppliers)
    • Authorized generic or license agreements

What generic or biosimilar suppliers compete with BRYNOVIN?

Answer: Not available from the provided input.

Why supplier mapping depends on the active ingredient

  • Competitive suppliers track the same INN across brands and strengths.

Where are BRYNOVIN shipments sourced from (distribution and logistics)?

Answer: Not available from the provided input.

Typical distribution data sources

  • Label and package insert “distributed by” entities
  • NDC wholesaler channel coverage
  • Regional importers tied to country-specific authorization

Key Takeaways

  • A supplier list for BRYNOVIN cannot be built from the provided input because “BRYNOVIN” alone does not uniquely identify the drug.
  • Supplier identification requires product identity (active ingredient and dosage form/strength) tied to authoritative label or regulatory records.
  • With that identity, a complete supplier map can be produced across API, finished dosage manufacturing, packaging/labeling, and distribution.

FAQs

  1. How do I find the API supplier behind a drug brand name?
  2. What label fields identify the finished-dose manufacturer and packager?
  3. How does an Orange Book entry change the supplier landscape?
  4. What’s the fastest way to map suppliers by NDC instead of brand name?
  5. How do contract manufacturing arrangements show up in regulatory documents?

References

  1. FDA. Drugs@FDA (Prescribing Information and Label).
  2. FDA. Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations.

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