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Glama

Govparse Government Data Gateway

fda_approvals_drugs

Which companies just won an FDA drug approval or supplement? Search openFDA drug/drugsfda applications by sponsor company, application type (NDA/ANDA/BLA), route, marketing status, most-recent approval date (since), or original market-entry date (first_approval_after). Returns the applicant company (entity-resolved where possible), brand/ingredient/dosage, and approval dates — a day-one commercial/partnership target list for pharma sellers and CROs. openFDA public-domain records. [price: $0.05/row]

Input Schema

TableJSON Schema
NameRequiredDescriptionDefault
sortNolatest_approval_date | original_approval_date :asc|:desc. Default latest_approval_date:desc.
limitNoMax rows (default 25, cap 100).
routeNoRoute-of-administration fragment.
sinceNoMost recent approval/supplement on/after this date (YYYY-MM-DD).
offsetNoRows to skip.
companyNoApplicant/sponsor company — suffix/punctuation-insensitive.
entity_idNoResolved employer entity UUID (pivots to business360).
application_typeNoNDA | ANDA | BLA (CSV).
marketing_statusNoPrescription | Over-the-counter | Discontinued.
first_approval_afterNoOriginal approval (market entry) on/after this date (YYYY-MM-DD) — surfaces new market entrants.

Schema Changelog

Changes observed during successful MCP inspections. Dates show when Glama detected each change.

  1. Added

TDQS

A4.1/5.0
Behavior4/5

Does the description disclose side effects, auth requirements, rate limits, or destructive behavior?

No annotations are provided, so the description carries the full burden. It discloses important behavioral traits: the data source ('openFDA public-domain records'), pricing ('$0.05/row'), and entity resolution for applicant companies. It also lists the returned fields (brand, ingredient, dosage, approval dates). No contradictions or hidden side effects are noted.

Agents need to know what a tool does to the world before calling it. Descriptions should go beyond structured annotations to explain consequences.

Conciseness4/5

Is the description appropriately sized, front-loaded, and free of redundancy?

The description is four sentences, each adding value. The first sentence sets the context, the second lists search fields, the third describes the output, and the fourth provides source and pricing. It is front-loaded and efficient, though the sentence about returns could be slightly more concise.

Shorter descriptions cost fewer tokens and are easier for agents to parse. Every sentence should earn its place.

Completeness4/5

Given the tool's complexity, does the description cover enough for an agent to succeed on first attempt?

Given the 10 parameters (none required) and no output schema, the description covers purpose, search criteria, return fields, and even pricing and data source. It is complete enough for an agent to understand when and how to use the tool, though a few more details on typical output structure would be beneficial.

Complex tools with many parameters or behaviors need more documentation. Simple tools need less. This dimension scales expectations accordingly.

Parameters3/5

Does the description clarify parameter syntax, constraints, interactions, or defaults beyond what the schema provides?

Schema description coverage is 100%, so the baseline is 3. The description adds minimal new meaning beyond the schema: it groups parameters by category (sponsor company, application type, etc.) and mentions 'suffix/punctuation-insensitive' for company, which is already in the schema. It does not significantly enhance understanding of the parameters.

Input schemas describe structure but not intent. Descriptions should explain non-obvious parameter relationships and valid value ranges.

Purpose5/5

Does the description clearly state what the tool does and how it differs from similar tools?

The description opens with a targeted question ('Which companies just won an FDA drug approval or supplement?') and clearly identifies the resource as FDA drug approvals/supplements. It lists specific searchable fields (sponsor company, application type, route, etc.) and distinguishes itself from sibling tools like fda_clearances_devices and fda_recalls_search by focusing exclusively on drugs.

Agents choose between tools based on descriptions. A clear purpose with a specific verb and resource helps agents select the right tool.

Usage Guidelines4/5

Does the description explain when to use this tool, when not to, or what alternatives exist?

The description explicitly states the searchable criteria and the intended use case ('a day-one commercial/partnership target list for pharma sellers and CROs'). While it does not directly state when not to use or name alternatives, the sibling tools are in different domains (devices, recalls, warning letters), so the usage context is implicitly clear.

Agents often have multiple tools that could apply. Explicit usage guidance like "use X instead of Y when Z" prevents misuse.

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TDQS

A4.2/5.0
Disambiguation5/5

Each tool targets a distinct domain and specific action (e.g., FDA approvals vs clearances vs recalls; firmstanding business360 dossier vs search vs screen). Even overlapping concepts like 'business360' vs 'business360_lookup' are distinguished by input (UUID vs name+state). No two tools appear to do the same thing.

Naming Consistency5/5

All tools use a consistent lowercase snake_case pattern with domain prefix (e.g., fda_*, firmstanding_*, fmcsa_*, govcon_*). Action words (search, lookup, screen, feed, stats) follow predictable usage. The naming is uniform and easy to parse.

Tool Count4/5

38 tools is on the higher end but appropriate for a comprehensive government data gateway spanning multiple agencies and datasets. Each domain has a reasonable number of tools (e.g., FMCSA: 7, OFLC: 6). Could potentially be trimmed slightly, but overall well-scoped for the stated purpose.

Completeness5/5

The tool surface covers the major government data sources comprehensively: FDA (approvals, clearances, recalls), FMCSA (carrier census, safety, insurance, etc.), FSIS, DOJ/OFLC, OSHA/EPA/DOL enforcement, SEC insider filings, clinical trials, VA facilities/opportunities/vendors, and federal contracting. No obvious gaps for the stated gateway purpose.

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