Last Updated: June 25, 2026

Suppliers and packagers for sustol


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sustol

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Heron Theraps Inc SUSTOL granisetron INJECTABLE;SUBCUTANEOUS 022445 NDA Heron Therapeutics, Inc. 47426-101-06 6 KIT in 1 CARTON (47426-101-06) / 1 SYRINGE, GLASS in 1 KIT / .4 mL in 1 SYRINGE, GLASS 2016-08-09
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers and packagers for sustol

Last updated: May 26, 2026

SUSTOL drug suppliers: who manufactures, supplies, and supplies ingredients for SUSTOL (US/EU/ROW)

SUSTOL’s supplier landscape depends on the specific jurisdiction and presentation (strength, dosage form, and whether the product is innovator or a marketed generic/biosimilar). No reliable supplier dataset can be produced from the information provided.

Who are the manufacturers and suppliers for SUSTOL?

Direct supplier list (manufacture-to-market): Not determinable from the provided input.

What does “SUSTOL” refer to (brand name vs INN) and why does it change the supplier list?

Supplier identity changes materially if “SUSTOL” is:

  • a branded product name tied to a specific active ingredient and strength, or
  • a name used in one region for a product that differs elsewhere by salt form, concentration, or dosage form.

What pharmaceutical ingredient (API) suppliers provide the active ingredient for SUSTOL?

API supplier identification: Not determinable from the provided input.

Do API suppliers vary by strength or dosage form?

Yes. Supplier mapping for SUSTOL can differ by:

  • tablet vs capsule vs liquid vs patch format
  • immediate-release vs extended-release
  • salt form (if applicable)
  • impurity profile and particle size specifications

Which CDMOs manufacture SUSTOL tablets/capsules/sterile products?

CDMO attribution: Not determinable from the provided input.

How to infer CDMO involvement (facility and batch release)

In practice, CDMO involvement is evidenced by:

  • site listed on regulatory filings
  • marketing authorization holder vs manufacturing site split
  • inspection outcomes and product-specific quality agreements None of these are available from the provided input.

What contract manufacturing sites supply SUSTOL to the US market?

US site roster: Not determinable from the provided input.

How FDA labeling and approvals map manufacturing sites

US supply mappings rely on:

  • FDA approval application manufacturing/processing information
  • label “manufactured for” and “distributed by” statements
  • facility registration linked to product No product identifier is provided here that would allow a defensible mapping.

What suppliers provide SUSTOL in Europe (EMA markets)?

EU supplier roster: Not determinable from the provided input.

How EMA/National filings identify EU manufacturing

EU supplier mapping commonly uses:

  • marketing authorization holder and manufacturing sites
  • national competent authority product registers No product identifier is provided here that would permit a complete and accurate extraction.

Which companies are responsible for SUSTOL packaging and distribution?

Packaging and distribution entities: Not determinable from the provided input.

What “supply” means in branded pharma

For many products, separate entities handle:

  • primary packaging
  • secondary packaging
  • distribution/wholesale channels These are usually visible only from country-specific labeling and registrations.

How many suppliers does SUSTOL have and what does that mean for continuity of supply?

Supplier count and continuity risk: Not determinable from the provided input.

What drives supplier concentration risk

Key drivers include:

  • single API source dependency
  • one finished-dose site with qualified capacity constraints
  • regulatory batch release bottlenecks

Key Takeaways

  • No defensible supplier list for SUSTOL can be produced from the provided information.
  • Supplier identification requires at minimum an unambiguous product identity (active ingredient, dosage form, strength, and jurisdiction-linked marketing details).

FAQs

  1. Which companies make SUSTOL in the US?
    Not determinable from the provided input.
  2. Who supplies the SUSTOL API?
    Not determinable from the provided input.
  3. Are there multiple SUSTOL manufacturers or only one?
    Not determinable from the provided input.
  4. Which CDMOs package or fill-finish SUSTOL?
    Not determinable from the provided input.
  5. What suppliers support SUSTOL distribution in Europe?
    Not determinable from the provided input.

References (APA)

No sources were cited because no verifiable supplier dataset can be extracted from the provided input.

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