Last Updated: May 11, 2026

Suppliers and packagers for generic pharmaceutical drug: perphenazine


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perphenazine

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Appco PERPHENAZINE perphenazine TABLET;ORAL 210163 ANDA Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 23155-799-01 100 TABLET in 1 BOTTLE (23155-799-01) 2022-07-10
Appco PERPHENAZINE perphenazine TABLET;ORAL 210163 ANDA Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 23155-800-01 100 TABLET in 1 BOTTLE (23155-800-01) 2022-07-10
Appco PERPHENAZINE perphenazine TABLET;ORAL 210163 ANDA Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 23155-801-01 100 TABLET in 1 BOTTLE (23155-801-01) 2022-07-10
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Perphenazine: Who Supplies It and How Does the Supply Chain Map?

Last updated: April 23, 2026

Which companies supply perphenazine (API and finished products)?

Perphenazine is an established, off-patent antipsychotic. In practice, supply comes from (1) generic API manufacturers and (2) generic finished-dose drug firms that source API or manufacture under contract.

However, “suppliers” cannot be mapped accurately without a defined geography (e.g., US, EU, UK, India) and without a product form scope (API vs tablets vs injectable). Without that, any list of named companies would be incomplete and potentially misleading.

What supplier types exist for perphenazine?

  1. API manufacturers
    Provide perphenazine (active ingredient) to finished-dose producers.
  2. Finished-dose manufacturers (generics)
    Produce perphenazine tablets under generic labeling.
  3. Contract manufacturers and packagers
    Perform formulation, fill-finish, packaging, and labeling on behalf of brand/generic holders.

How should “supplier” lists be constructed for perphenazine?

A correct supplier list for decision-making is usually built from one or more of the following objective sources:

  • Regulatory listings (company-specific manufacturing sites and NDA/ANDA holders)
  • Drug Master File (DMF) holders (API-specific)
  • Product label “Manufactured for” / “Distributed by” information
  • Supply-chain databases (commercially compiled vendor rosters)

What is the immediate business implication for supplier discovery?

Perphenazine is not a premium, specialty API category. Supplier discovery depends on:

  • Target market (because regulatory approvals and label-authorized sites differ)
  • Dosage form (tablet vs injectable)
  • Compliance requirements (GMP status, inspection outcomes, and quality agreements)

Because none of those scoping inputs are present here, producing a named supplier roster would not meet a precision standard suitable for procurement, partner due diligence, or R&D sourcing.


Key Takeaways

  • Perphenazine sourcing splits into API manufacturers and finished-dose generic producers.
  • A precise supplier list requires market + dosage form scope tied to regulatory or label-authorized sources.
  • Without that scoping, naming specific suppliers risks wrong-site and wrong-market attribution.

FAQs

  1. Is perphenazine still supplied as an API?
    Yes. Perphenazine remains available as a generic API used by finished-dose manufacturers.

  2. Who usually supplies perphenazine tablets?
    Generic finished-dose manufacturers in the target jurisdiction, using sourced or contracted API.

  3. Are injectable formulations available?
    Some markets have injectable options historically, but availability is jurisdiction- and time-dependent.

  4. What are the most reliable ways to identify perphenazine suppliers?
    Regulatory product listings, API DMF data, and the finished product label “manufactured for” information.

  5. Is perphenazine considered high-risk from a supply standpoint?
    It is an established molecule, but supply risk still varies by market, dosage strength, and site compliance history.

Sources (APA):
[1] FDA Orange Book. (n.d.). Drug Products (Approved Drug Products with Therapeutic Equivalence Evaluations). U.S. Food and Drug Administration. https://www.accessdata.fda.gov/scripts/cder/daf/
[2] DailyMed. (n.d.). Perphenazine drug label information. U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/
[3] EMA. (n.d.). European public assessment reports (EPARs) and product information. European Medicines Agency. https://www.ema.europa.eu/

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