Get an FDA record

curl --request GET \
  --url https://api.pav.bio/v1/fda/{record_key} \
  --header 'Authorization: Bearer <token>'

const options = {method: 'GET', headers: {Authorization: 'Bearer <token>'}};

fetch('https://api.pav.bio/v1/fda/{record_key}', options)
  .then(res => res.json())
  .then(res => console.log(res))
  .catch(err => console.error(err));

package main

import (
	"fmt"
	"net/http"
	"io"
)

func main() {

	url := "https://api.pav.bio/v1/fda/{record_key}"

	req, _ := http.NewRequest("GET", url, nil)

	req.Header.Add("Authorization", "Bearer <token>")

	res, _ := http.DefaultClient.Do(req)

	defer res.Body.Close()
	body, _ := io.ReadAll(res.Body)

	fmt.Println(string(body))

}

{
  "record_key": "purple_book_product:761508:001",
  "record_type": "purple_book_product",
  "source": "purple_book",
  "title": "GENGLYCOS",
  "source_version": "2026-08",
  "fda_organization_name": "Regeneron Pharmaceuticals, Inc.",
  "company": {
    "company_id": 5093,
    "short_name": "regeneron",
    "name": "Regeneron Pharmaceuticals"
  },
  "application_key": "BLA:761508",
  "product_key": "BLA:761508:001",
  "designation_id": "1186826",
  "patent_number": "10022461",
  "description": "<string>",
  "document_date": "2023-12-25",
  "event_date": "2023-12-25",
  "event_date_type": "patent_expiry",
  "status": "RX",
  "source_url": "<string>",
  "details": {
    "ingredient": "SEMAGLUTIDE",
    "strength": "300MG/5ML (60MG/ML)",
    "dosage_route": "TABLET;ORAL",
    "dosage_form": "Injection",
    "route": "Intravenous",
    "therapeutic_equivalence_code": "AB1",
    "reference_listed_drug": true,
    "reference_standard": true,
    "patent_use_code": "U-4597",
    "pediatric_extension": true,
    "drug_substance_claim": true,
    "drug_product_claim": true,
    "license_type": "351(a)",
    "licensure": "Licensed",
    "license_number": "1760",
    "orphan_exclusivity_expiry": "2023-12-25",
    "reference_product_exclusivity_expiry": "2023-12-25",
    "approval_date_raw": "Approved Prior to Jan 1, 1982",
    "generic_name": "inosine pranobex",
    "designation_withdrawn_date": "2023-12-25",
    "approvals": [
      {
        "marketing_approval_date": "2023-12-25",
        "exclusivity_end_date": "2023-12-25",
        "trade_name": "Darzalex",
        "generic_name": "daratumumab",
        "approved_labeled_indication": "<string>",
        "protected_indication": "<string>"
      }
    ],
    "brand": "Baxter",
    "reason": "Mislabeling",
    "reason_description": "<string>",
    "product_types": [
      "Drugs"
    ],
    "issuing_office": "Center for Drug Evaluation and Research (CDER)",
    "fda_reference_id": "738238",
    "closeout_date": "2023-12-25",
    "application_type": "NDA",
    "products": "NUBEQA",
    "submission_count": 123,
    "latest_submission": {
      "submission_type": "SUPPL",
      "submission_number": "16",
      "status": "AP",
      "status_date": "2023-12-25",
      "submission_class": "Labeling",
      "review_priority": "PRIORITY",
      "notes": "<string>"
    },
    "letter_type": "COMPLETE RESPONSE",
    "application_numbers": [
      "NDA 218705"
    ],
    "category": "cancer",
    "current_status": "Traditional Approval Granted (12/16/2022)",
    "confirmatory_requirements": [
      {
        "requirement": "<string>",
        "projected_completion": "2023-12-25"
      }
    ],
    "center": "Center for Drug Evaluation and Research",
    "meeting_start": "2023-11-07T05:31:56Z",
    "meeting_end": "2023-11-07T05:31:56Z",
    "documents": [
      {
        "title": "<string>",
        "url": "<string>",
        "document_type": "<string>",
        "document_date": "2023-12-25"
      }
    ]
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

GET

fda

{record_key}

Get an FDA record

curl --request GET \
  --url https://api.pav.bio/v1/fda/{record_key} \
  --header 'Authorization: Bearer <token>'

const options = {method: 'GET', headers: {Authorization: 'Bearer <token>'}};

fetch('https://api.pav.bio/v1/fda/{record_key}', options)
  .then(res => res.json())
  .then(res => console.log(res))
  .catch(err => console.error(err));

package main

import (
	"fmt"
	"net/http"
	"io"
)

func main() {

	url := "https://api.pav.bio/v1/fda/{record_key}"

	req, _ := http.NewRequest("GET", url, nil)

	req.Header.Add("Authorization", "Bearer <token>")

	res, _ := http.DefaultClient.Do(req)

	defer res.Body.Close()
	body, _ := io.ReadAll(res.Body)

	fmt.Println(string(body))

}

{
  "record_key": "purple_book_product:761508:001",
  "record_type": "purple_book_product",
  "source": "purple_book",
  "title": "GENGLYCOS",
  "source_version": "2026-08",
  "fda_organization_name": "Regeneron Pharmaceuticals, Inc.",
  "company": {
    "company_id": 5093,
    "short_name": "regeneron",
    "name": "Regeneron Pharmaceuticals"
  },
  "application_key": "BLA:761508",
  "product_key": "BLA:761508:001",
  "designation_id": "1186826",
  "patent_number": "10022461",
  "description": "<string>",
  "document_date": "2023-12-25",
  "event_date": "2023-12-25",
  "event_date_type": "patent_expiry",
  "status": "RX",
  "source_url": "<string>",
  "details": {
    "ingredient": "SEMAGLUTIDE",
    "strength": "300MG/5ML (60MG/ML)",
    "dosage_route": "TABLET;ORAL",
    "dosage_form": "Injection",
    "route": "Intravenous",
    "therapeutic_equivalence_code": "AB1",
    "reference_listed_drug": true,
    "reference_standard": true,
    "patent_use_code": "U-4597",
    "pediatric_extension": true,
    "drug_substance_claim": true,
    "drug_product_claim": true,
    "license_type": "351(a)",
    "licensure": "Licensed",
    "license_number": "1760",
    "orphan_exclusivity_expiry": "2023-12-25",
    "reference_product_exclusivity_expiry": "2023-12-25",
    "approval_date_raw": "Approved Prior to Jan 1, 1982",
    "generic_name": "inosine pranobex",
    "designation_withdrawn_date": "2023-12-25",
    "approvals": [
      {
        "marketing_approval_date": "2023-12-25",
        "exclusivity_end_date": "2023-12-25",
        "trade_name": "Darzalex",
        "generic_name": "daratumumab",
        "approved_labeled_indication": "<string>",
        "protected_indication": "<string>"
      }
    ],
    "brand": "Baxter",
    "reason": "Mislabeling",
    "reason_description": "<string>",
    "product_types": [
      "Drugs"
    ],
    "issuing_office": "Center for Drug Evaluation and Research (CDER)",
    "fda_reference_id": "738238",
    "closeout_date": "2023-12-25",
    "application_type": "NDA",
    "products": "NUBEQA",
    "submission_count": 123,
    "latest_submission": {
      "submission_type": "SUPPL",
      "submission_number": "16",
      "status": "AP",
      "status_date": "2023-12-25",
      "submission_class": "Labeling",
      "review_priority": "PRIORITY",
      "notes": "<string>"
    },
    "letter_type": "COMPLETE RESPONSE",
    "application_numbers": [
      "NDA 218705"
    ],
    "category": "cancer",
    "current_status": "Traditional Approval Granted (12/16/2022)",
    "confirmatory_requirements": [
      {
        "requirement": "<string>",
        "projected_completion": "2023-12-25"
      }
    ],
    "center": "Center for Drug Evaluation and Research",
    "meeting_start": "2023-11-07T05:31:56Z",
    "meeting_end": "2023-11-07T05:31:56Z",
    "documents": [
      {
        "title": "<string>",
        "url": "<string>",
        "document_type": "<string>",
        "document_date": "2023-12-25"
      }
    ]
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

{
  "error": {
    "code": "not_found",
    "message": "program 999999 not found",
    "request_id": "3f2b9c1d8a7e4f6b9c0d1e2f3a4b5c6d"
  }
}

Authorizations

Authorization

string

header

required

Use a personal or organization Pav API key from Pav developer settings. Send it as Authorization: Bearer <api_key>.

Path Parameters

record_key

string

required

record_key from a list response. May contain /, : and spaces.

Maximum string length: 400

Example:

"purple_book_product:761508:001"

Response

Successful Response

record_key

string

required

Durable key built from FDA identifiers; use it with GET /v1/fda/{record_key}.

Example:

"purple_book_product:761508:001"

record_type

enum<string>

required

Kind of FDA record.

Available options:

orange_book_product,

orange_book_patent,

orange_book_exclusivity,

purple_book_product,

orphan_designation,

warning_letter,

recall,

drug_application,

complete_response_letter,

accelerated_approval,

advisory_committee_meeting

Example:

"purple_book_product"

source

string

required

FDA publication the record comes from.

Example:

"purple_book"

title

string

required

Display title: trade name, patent label, letter subject or recalled product.

Example:

"GENGLYCOS"

source_version

string | null

Source edition: YYYY-MM for Orange and Purple Book, the load date for orphan designations, null for continuously published sources.

Example:

"2026-08"

fda_organization_name

string | null

Applicant, sponsor or recipient name as FDA spells it.

Example:

"Regeneron Pharmaceuticals, Inc."

company

FdaCompany · object | null

The linked company; null when the FDA name is not linked.

Show child attributes

application_key

string | null

FDA application: N: (NDA), A: (ANDA) or BLA: plus the number.

Example:

"BLA:761508"

product_key

string | null

Application plus the FDA product number.

Example:

"BLA:761508:001"

designation_id

string | null

FDA orphan designation id; there is one record per designation.

Example:

"1186826"

patent_number

string | null

Orange Book listed US patent number.

Example:

"10022461"

description

string | null

Ingredient for products, patents and exclusivities; indication for orphan designations; subject or reason for letters and recalls.

document_date

string<date> | null

Date FDA issued the record (approval, letter, recall, designation).

event_date

string<date> | null

The date event_date_type names, e.g. a patent expiry.

event_date_type

string | null

What event_date is: approval, patent_expiry, exclusivity_expiry, orphan_exclusivity_expiry, or another event.

Example:

"patent_expiry"

status

string | null

Source status: marketing status for products (RX, OTC, DISCN), listed or delisted for patents, the code for exclusivities, the latest action otherwise.

Example:

"RX"

source_url

string | null

Official FDA page for the record. Orange Book patents and exclusivities link to their product's patent and exclusivity page.

details

FdaRecordDetails · object

Record-type specific source fields.

Show child attributes

Overview

Search

Programs

Drugs

Companies

Trials

Deals

Patents

FDA

Changes

Stats

Get an FDA record

Authorizations

Path Parameters

Response