Last Updated: May 3, 2026

METHAZOLAMIDE Drug Patent Profile


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Which patents cover Methazolamide, and when can generic versions of Methazolamide launch?

Methazolamide is a drug marketed by Ajanta Pharma Ltd, Anda Repository, Ani Pharms, Applied Anal, Athem, Bausch And Lomb Inc, Chartwell Rx, and Tagi. and is included in eight NDAs.

The generic ingredient in METHAZOLAMIDE is methazolamide. There are seven drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the methazolamide profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Methazolamide

A generic version of METHAZOLAMIDE was approved as methazolamide by ANI PHARMS on June 30th, 1993.

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Summary for METHAZOLAMIDE
US Patents:0
Applicants:8
NDAs:8

US Patents and Regulatory Information for METHAZOLAMIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Ajanta Pharma Ltd METHAZOLAMIDE methazolamide TABLET;ORAL 217408-001 Feb 9, 2026 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Applied Anal METHAZOLAMIDE methazolamide TABLET;ORAL 040011-001 Jul 17, 1997 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Anda Repository METHAZOLAMIDE methazolamide TABLET;ORAL 040062-002 Jan 27, 1994 AB RX No Yes ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Bausch And Lomb Inc METHAZOLAMIDE methazolamide TABLET;ORAL 207438-002 Oct 5, 2018 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Applied Anal METHAZOLAMIDE methazolamide TABLET;ORAL 040011-002 Jul 17, 1997 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Tagi METHAZOLAMIDE methazolamide TABLET;ORAL 215615-002 Oct 18, 2022 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Methazolamide (Oral Acetazolamide Analog): Investment Scenario and Fundamentals Analysis

Last updated: April 23, 2026

What is methazolamide and how is it used?

Methazolamide (CAS 59-14-3) is an oral carbonic anhydrase inhibitor used primarily for glaucoma (ocular hypertension) and for altitude sickness prophylaxis and treatment in some jurisdictions. It is also used in off-label settings where carbonic anhydrase inhibition is clinically relevant (e.g., certain acid-base disorders), but its core commercial positioning remains ophthalmic and rescue-oriented indications tied to carbonic anhydrase pharmacology.

Drug class

  • Carbonic anhydrase inhibitor (systemic oral)

Typical clinical roles cited in regulatory/clinical references

  • Glaucoma and related intraocular pressure reduction
  • Altitude sickness prophylaxis (and sometimes treatment)

Key practical profile

  • Oral, small molecule, established mechanism
  • Legacy therapy with patent-life typically long past in major markets (pricing and supply risk matter more than pipeline optionality)

What is the competitive landscape for methazolamide?

Methazolamide is a legacy, off-patent drug in most markets. Competitive pressure is dominated by:

  • Generic manufacturers (multiple ANDA or local equivalents across geographies)
  • Supplier stability (raw material sourcing and batch consistency)
  • Product form factors (tablet strength and excipient/package alignment)
  • Price compression driven by generic entry

Market behavior for off-patent carbonic anhydrase inhibitors

  • Chronic or episodic use creates repeat demand but limited willingness to pay premium pricing
  • Tender-driven hospital/offtake cycles reduce margin volatility only if a supplier retains contract status
  • Brand-like differentiation is uncommon; bioequivalence compliance and manufacturing reliability dominate

Direct competitive set

  • Carbonic anhydrase inhibitors used for similar therapeutic aims: acetazolamide and other class members depending on market availability and guideline preferences (e.g., acetazolamide often has wider penetration)

Acetazolamide is frequently more commonly used in many countries, which can cap methazolamide’s addressable share when clinicians prefer an entrenched alternative.

What do the fundamentals say about market attractiveness?

For an investor, methazolamide behaves like a “value chain” bet rather than an “R&D upside” bet. The fundamentals are driven by supply, generic pricing, and regulatory continuity.

Demand drivers

  • Ocular pressure management: steady but not rapidly growing; affected by ophthalmology prescribing patterns and availability of preferred alternatives
  • Altitude sickness: seasonal and travel-linked demand with periodic surges around travel peaks
  • Clinical substitution risk: carbonic anhydrase inhibitors are substitutable at the class level in many settings; clinician preference and country guidelines determine which molecule wins

Pricing and margin drivers

  • Generic price erosion is a structural feature
  • Margins depend on:
    • Whether the investor controls a low-cost manufacturing route
    • Contract manufacturing or owned production capacity
    • Ability to avoid stock-outs (lost sales during shortages can be hard to regain)

Risk factors that matter for a legacy oral drug

  • Batch failures and regulatory actions can trigger immediate revenue loss
  • Raw material and intermediates cost volatility
  • Competitors undercut pricing when supply is ample
  • Formulation and packaging updates can require relabeling work and minor compliance overhead

What does the patent and exclusivity reality imply for investors?

Methazolamide is a mature product. The investment implication is that traditional patent-based defensibility is typically not the primary value lever. Returns come from:

  • Manufacturing scale and cost
  • Regulatory execution (no downtime)
  • Contracting and channel control
  • Speed to maintain market supply when competitors fail or exit

Because the patent landscape is country-specific and changes with filings and expirations, the most actionable approach for investors is to treat methazolamide as a commercial manufacturing and distribution thesis rather than a line-extension thesis.

How should the investment case be framed: manufacturing and supply vs. pipeline?

Investment thesis (commercial)

  • Supply reliability edge: build or buy capacity that ensures continuity of supply in key tenders and distributor inventories
  • Cost-positioning: secure low-COGS manufacturing and stable API sourcing
  • Portfolio role: position methazolamide as a stable, cash-generative legacy SKU that de-risks a broader portfolio, while keeping option value for reformulations

Investment thesis (R&D optionality)

Methazolamide’s R&D upside is constrained by off-patent status, but investors can still pursue value creation through:

  • Line extensions where allowed (new formulations, alternate delivery, combination products where regulatory pathways permit)
  • Manufacturing improvements that support premium pricing in certain channels (e.g., consistent supply and tighter specs)

In practice, line-extension returns are usually smaller than manufacturing and market access returns for this molecule.

What do regulatory and labeling references indicate about the product’s commercial scope?

Regulatory references in standard drug databases identify methazolamide as a systemic carbonic anhydrase inhibitor with established clinical uses in glaucoma and altitude sickness contexts. These uses support baseline demand but do not indicate high-growth novelty.

Labeling and drug references

  • Standard pharmacology references classify methazolamide as a carbonic anhydrase inhibitor and document its therapeutic uses in glaucoma and altitude sickness contexts (as reflected across major drug information compendia). Examples include drug monographs and drug databases that summarize mechanism and indications. [1,2]

Where can methazolamide win share?

Share gains in an off-patent legacy drug usually come from execution, not differentiation.

Commercial levers

  • Secure procurement contracts in markets where methazolamide remains a preferred option
  • Maintain inventory discipline to reduce stock-out risk for travel seasonal peaks
  • Provide consistent tablet strength supply aligned to local prescribing patterns
  • Use distribution relationships to keep shelf presence in ophthalmic channels

Competitive tactics

  • If acetazolamide is the dominant class option, methazolamide wins by:
    • Competitive pricing in tenders
    • Better availability or fewer supply interruptions
    • Favorable reimbursement terms

What are the key diligence items before capital deployment?

A methazolamide investment needs a due-diligence checklist that prioritizes production continuity and compliance.

Manufacturing and compliance

  • Current GMP status for the manufacturing site(s) producing methazolamide
  • Batch history: out-of-spec rates, deviations, recalls, and CAPA closure timelines
  • API sourcing continuity (and whether second-source API exists)
  • Tablet formulation consistency and stability data for commercial strengths

Regulatory and market access

  • Country-level registration status and renewal cadence
  • Ability to sustain bioequivalence documentation if required for line refreshes
  • Tender history: win rate, contract duration, and penalty clauses tied to supply

Competitive economics

  • Latest market pricing trend by country and channel (hospital vs retail)
  • Competitor shipment volumes and signs of capacity exits
  • Whether pricing is moving due to cost drivers (API, excipients, logistics) or pure competition

Investment scenario modeling (how returns typically form for legacy methazolamide)

A practical scenario approach for methazolamide focuses on volume and price spread plus downtime.

Base case (most common for off-patent generics)

  • Stable demand
  • Competitive pricing pressure
  • Margin supported by cost position and manufacturing reliability
  • Returns track execution more than growth

Upside case

  • Competitor supply disruption or regulatory action opens procurement slots
  • Investor secures additional tenders or expands distributor coverage
  • Margin improves briefly through reduced price competition while demand is “unsatisfied”

Downside case

  • Price compression accelerates due to new entrants
  • Manufacturing downtime reduces available supply, causing loss of repeat orders
  • Regulatory issues trigger shipment holds and delayed revenue recognition

For methazolamide, “upside” is typically supply-availability driven, not technology driven.

What does a commercialization plan look like for investors?

Commercial strategy

  • Anchor on one or two high-demand geographies where methazolamide remains in formularies or is regularly procured
  • Lock long-duration supply agreements to smooth seasonal demand
  • Maintain safety stock tied to procurement lead times to prevent lost contracts

Operational strategy

  • Use a second API source strategy
  • Standardize tablet packaging to reduce relabeling risk
  • Run continuous improvement around yield and batch acceptance rate to lower landed cost

Portfolio strategy

  • Treat methazolamide as a cashflow stabilizer
  • Allocate incremental R&D budget only to tightly defined, low-variance regulatory projects (if any) with a realistic path to market differentiation

Key Takeaways

  • Methazolamide is a legacy, off-patent carbonic anhydrase inhibitor with primary use in glaucoma and altitude sickness contexts, and it typically trades like a generic supply and cost thesis rather than an IP-led growth story. [1,2]
  • Investment returns are driven by manufacturing reliability, regulatory continuity, and procurement contracting in a price-compressed generic market.
  • The most actionable “upside” scenario is competitor supply disruption or procurement capture, not molecule-level differentiation.
  • Diligence should prioritize GMP execution, batch performance, API sourcing resilience, and tender economics.
  • For portfolio investors, methazolamide is usually best treated as a stable cashflow SKU, with limited R&D optionality.

FAQs

Is methazolamide a patent-protected growth opportunity?

No. It is a mature, off-patent product in most markets, so defensibility usually comes from operational execution and market access rather than new IP.

What drives demand for methazolamide?

Demand comes from established clinical use in glaucoma management and altitude sickness prophylaxis/treatment, with seasonal effects for travel-linked use.

How do investors make money on legacy methazolamide?

By sustaining competitive landed costs, avoiding supply disruptions, and winning/retaining procurement contracts in channels where the product is listed and repeatedly purchased.

Who are the main competitive threats?

Generic carbonic anhydrase inhibitor alternatives, especially acetazolamide where it has higher utilization, plus other manufacturers competing on price and supply reliability.

What are the biggest operational risks?

Manufacturing downtime, regulatory quality events, API supply interruptions, and stock-outs that lead to lost repeat orders during procurement cycles.


References

[1] DrugBank Online. Methazolamide. DrugBank database entry. https://go.drugbank.com/
[2] DailyMed. Methazolamide drug label information. U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/

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