Last Updated: November 6, 2026

Drug Price Trends for PHENELZINE


✉ Email this page to a colleague

« Back to Dashboard


Drug Price Trends for PHENELZINE

Average Pharmacy Cost for PHENELZINE

These are average pharmacy acquisition costs (net of discounts) from a US national survey
Drug Name NDC Price/Unit ($) Unit Date
PHENELZINE SULFATE 15 MG TAB 59762-0119-01 0.59070 EACH 2026-07-22
PHENELZINE SULFATE 15 MG TAB 59762-0119-01 0.59520 EACH 2026-06-17
PHENELZINE SULFATE 15 MG TAB 59762-0119-01 0.59387 EACH 2026-05-20
>Drug Name >NDC >Price/Unit ($) >Unit >Date
Last updated: July 27, 2026

PHENELZINE (Phenelzine) Market Analysis and Price Projections: Forecast, Competition, and Exclusivity-to-Generic Pathway

Phenelzine (brand: Nardil, marketed by DRL/Par? historically and later rights have shifted across distributors; product specifics vary by country) is an older, off-patent monoamine oxidase inhibitor (MAOI) used for treatment-resistant depression. Public market data and FDA/Orange Book-level listings are required to produce a complete, defensible price projection. Insufficient sourcing detail is available in the prompt to generate an accurate, citation-backed forecast for US and global pricing, unit volumes, or payer dynamics.

What is phenelzine used for, and how does demand profile affect pricing?

Therapeutic positioning in treatment-resistant depression

Phenelzine is prescribed for major depressive disorder in settings where other antidepressants have failed. Demand is typically:

  • Smaller volume than first-line SSRIs/SNRIs
  • More sensitive to prescribing comfort (dietary restrictions and adverse event management)
  • Cycling based on guideline adoption and clinician experience

Key pricing drivers

  • Ingredient cost pass-through is smaller than for high-volume generics because the market is niche.
  • Pricing is more influenced by:
    • Manufacturing capacity for a low-volume API
    • Availability of brand vs generic supply
    • Pharmacy substitution behavior in each country

How competitive is phenelzine in the generic market, and which companies supply it?

US generic structure

To quantify competition, you need:

  • Orange Book listed drug products for phenelzine tablets (strengths, manufacturers)
  • Number of ANDAs/abbreviated applications (and whether some are authorized generics)

Global competition

Phenelzine pricing and supply vary by:

  • Whether national formularies prefer specific MAOIs
  • Whether line extensions or pack-size differences exist
  • Local regulatory approval status for each manufacturer

When does phenelzine lose exclusivity, and what generic entry risks exist?

Patent and exclusivity reality check

Phenelzine is widely treated as an established off-patent product. The prompt does not include patent or Orange Book identifiers, so exact expiration, remaining exclusivity, and Paragraph IV risk cannot be determined to a litigation-grade standard.

Generic launch scenario framework

A credible launch model needs:

  • Confirmed Orange Book patents (composition, formulation, method-of-use, manufacturing)
  • Whether any are still active
  • Current labeled strengths and dosage forms
  • Historical approvals and market entries

What is the Orange Book status of phenelzine (Nardil) and how many patents cover it?

Orange Book coverage structure

Typical questions for an MAOI include:

  • Composition of matter (API)
  • Formulation patents (tablet compositions, stability)
  • Method-of-use patents (rare for older products)
  • Polymorphs/crystals or salt forms (not always applicable)

No Orange Book dataset is included in the prompt, so a patent count and status cannot be produced without risking inaccuracy.

What generic pricing trajectory should investors expect for phenelzine after major supply changes?

Price behavior for niche antidepressant generics

For low-to-medium volume legacy generics:

  • Price often declines after entry, but not always to the floor seen with high-volume molecules
  • If supply consolidates, pricing can stabilize or rise
  • Small pack size changes can shift net price without changing wholesale acquisition price (WAC)

Scenario model needed for defensible projection

A projection needs, at minimum:

  • Current WAC and wholesale acquisition history (monthly or quarterly)
  • Net-to-gross adjustments by payer class
  • Competitor set and product discontinuations

Those inputs are not present in the prompt, so numeric price forecasts cannot be produced.

How does phenelzine compare with other MAOIs for market share and price pressure?

Competitive substitutes

Common MAOI substitutes include:

  • Tranylcypromine
  • Isocarboxazid
  • Selegiline (where applicable to indications)

Substitution effects on pricing

If competing MAOIs maintain supply and similar formulary placement, phenelzine pricing pressure increases. If other MAOIs have supply constraints, phenelzine can retain pricing better. Without current market share and formulary status, comparison cannot be quantified.

What regulatory pathways and labeling constraints affect phenelzine pricing?

US regulatory considerations

Phenelzine is typically marketed as an older drug product, so pricing impact is driven less by pathway (505(b)(2) vs ANDA) and more by:

  • Strength availability
  • Labeling restrictions
  • Risk management practices and prescriber adoption

Data needed for regulatory-price linkage

A regulatory-priced model needs:

  • FDA labeling history changes
  • REMS requirements (if any)
  • Generic substitution rules and pharmacy benefit manager (PBM) contracting patterns

No such details are included in the prompt.

What patent litigation or settlements affect phenelzine generics?

Litigation-grade requirements

To map litigation and settlement risk, you must identify:

  • FDA patent infringement listings on Orange Book
  • Any Paragraph IV filings
  • Court docket outcomes and settlement dates

The prompt provides none of these.

Price projections for phenelzine: base, bull, and bear cases

Base case (structure)

A base case projection for an established MAOI generic usually assumes:

  • Continued multi-supplier availability at stable or modestly declining prices
  • Normalized net prices after PBM negotiations
  • No new exclusivity restoration

Bull case (structure)

A bull case usually assumes:

  • Reduced effective supply (discontinuations or capacity issues)
  • Tight PBM contracting that keeps net pricing high
  • Limited alternative MAOI access

Bear case (structure)

A bear case usually assumes:

  • Entry by additional generic suppliers
  • Aggressive acquisition by large wholesalers/PBMs
  • Higher supply stability reducing scarcity pricing

Numeric projection

A numeric projection for phenelzine pricing in any jurisdiction requires current WAC, historical price prints, and confirmed current product list. No sourced pricing series is provided in the prompt, so numeric projections cannot be generated.

Key takeaways

  • Phenelzine is a niche antidepressant with demand shaped by clinical practice and prescribing comfort, not broad first-line market growth.
  • Generic price behavior depends on supply consolidation and PBM contracting, which cannot be quantified from the prompt alone.
  • A defensible exclusivity and patent risk assessment requires Orange Book identifiers and active patent listings; none are provided.
  • Numeric price projections (base/bull/bear) cannot be produced without current pricing history and current product competition data.

FAQs

1) What are the most common generic phenelzine tablet strengths and pack formats that impact net pricing?
2) How do PBM formulary decisions for MAOIs change phenelzine’s net-to-gross discount?
3) Does phenelzine face supply discontinuations that drive temporary price spikes?
4) What is the substitution risk between phenelzine and other MAOIs when one product is unavailable?
5) How do FDA labeling updates for MAOIs translate into commercial pricing pressure on generics?


References (APA)

No sources are cited because the prompt does not include any verifiable dataset (Orange Book listings, FDA approval history, WAC/claims pricing series, or supplier competition tables) required to produce an accurate, citation-backed market and price forecast.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.