Last Updated: August 9, 2026

Suppliers and packagers for generic pharmaceutical drug: finafloxacin


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finafloxacin

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Fonseca Biosciences XTORO finafloxacin SUSPENSION/DROPS;OTIC 206307 NDA Fonseca Biosciences, LLC 83709-001-01 1 BOTTLE, DROPPER in 1 CARTON (83709-001-01) / 5 mL in 1 BOTTLE, DROPPER 2026-05-01
Fonseca Biosciences XTORO finafloxacin SUSPENSION/DROPS;OTIC 206307 NDA Fonseca Biosciences, LLC 83709-001-90 1 POUCH in 1 CARTON (83709-001-90) / 1 BOTTLE, DROPPER in 1 POUCH / 1.5 mL in 1 BOTTLE, DROPPER 2026-05-01
Fonseca Biosciences XTORO finafloxacin SUSPENSION/DROPS;OTIC 206307 NDA Fonseca Biosciences, LLC 83709-001-91 1 BOTTLE, DROPPER in 1 CARTON (83709-001-91) / 5 mL in 1 BOTTLE, DROPPER 2026-05-01
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers for FINAFLOXACIN

Last updated: May 4, 2026

What qualifies as a “supplier” for finafloxacine?

“Suppliers” for a pharmaceutical drug can mean at least one of the following: (1) API manufacturers (finafloxacine active pharmaceutical ingredient), (2) intermediates providers used to make the API, (3) finished-dose manufacturers that hold the right to produce tablets/capsules/sterile products, and (4) traders/distributors that move catalog API through distribution channels.

A complete supplier map requires the target market (regulatory territory), dosage form, and whether the scope is API or finished product. No source set was provided that identifies finafloxacine-specific approved suppliers, dossiers, or commercial distribution routes.

Which finafloxacine suppliers are verifiably identifiable from the supplied information?

No finafloxacine supplier names, corporate entities, dossier references, regulatory filings, or catalog listings were provided in the prompt. Without those inputs or a cited source base, a complete and accurate supplier list cannot be produced.

Why a supplier list cannot be produced from the prompt alone

A supplier list for an API must be anchored to verifiable identifiers such as:

  • Regulatory approvals (e.g., US FDA Orange Book listings, EU EMA EPAR/PIP or national approvals, UK MHRA references)
  • Drug master files (DMFs) and letter-of-access references
  • Approved manufacturing sites tied to specific strengths and dosage forms
  • Commercial catalog evidence (e.g., CoA-bearing supplier pages that explicitly name finafloxacine as the listed API)

None of these are present in the provided message.

Key Takeaways

  • A supplier list for FINAFLOXACIN / finafloxacine cannot be generated accurately without verifiable source evidence tying specific companies to the API or finished product.
  • A correct supplier map must specify API vs finished dose and regulatory territory to avoid misattribution.

FAQs

  1. Can I get finafloxacine API suppliers from general antibiotic supplier lists?
    No. Generic supplier lists do not provide substance-specific confirmation that the exact API is finafloxacine.

  2. Does “supplier” mean API manufacturer or distributor?
    Both exist, but they are not interchangeable. API manufacturers and distributors have different verification requirements.

  3. How do you confirm a company supplies finafloxacine?
    Through regulatory listings (where applicable), DMF references, or CoA-bearing listings explicitly naming finafloxacine.

  4. Do intermediates suppliers qualify as finafloxacine suppliers?
    They qualify only for intermediate sourcing, not for direct API supply commitments.

  5. Can finafloxacine be spelled differently across documents?
    Yes. Product and substance naming variations can change search results and cause false matches if not normalized to the correct substance name.

Cited sources:
None.

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